Private Label Product Catalog

Private label supplier for all national retail pharmacy chains

Product Catalog

Ranitidine 150 mg

Pharmascience Inc., 6111, Royalmount Avenue, Suite 100, Montréal (QC), Canada H4P 2T4

Zantac is a registered trademark of GlaxoSmithKline

1

ZANTAC®

Strength DIN/NPN Format National Brand Reference Shelf Life

150 mg 02293471Blistered 8 countBlistered 24 countBottled 50 count

24 Months

ACTIVE INGREDIENTS: Each tablet contains: 150 mg of Ranitidine,

as Ranitidine Hydrochloride.

Colloidal Silicon Dioxide, Croscarmellose Sodium, Iron Oxide Red, Iron Oxide Yellow,Magnesium Stearate, Microcrystalline Cellulose, Polyvinyl Alcohol, Soy Lecithin, Talc,

Titanium Dioxide, Xanthan Gum

Medicinal Ingredient Non-Medicinal Ingredients

Unscheduled for adult use. In package sizes containing

no more than 4,500 mg. Schedule III if over

4,500 mg

Unscheduled for adult use. In package sizes containing

no more than 4,500 mg. Schedule III if over

4,500 mg

Unscheduled for adult use. In package sizes containing

no more than 4,500 mg. Schedule III if over

4,500 mg

Unscheduled for adult use. In package sizes containing

no more than 4,500 mg. Schedule III if over

4,500 mg

Unscheduled for adult use. In package sizes containing

no more than 4,500 mg. Schedule III if over

4,500 mg

Unscheduled for adult use. In package sizes containing

no more than 4,500 mg. Schedule III if over

4,500 mg

NWT (Follows Napra National)

BC Alberta Manitoba (Follows Napra National)

Saskatchewan (Follows Napra National)

Ontario (Follows Napra National)

Quebec New Brunswick (Follows Napra National)

PEI (Follows Napra National)

Nova Scotia (Follows Napra National)

Nfld Yukon (Follows Napra National)

Annexe 3

Unscheduled for adult use. In package sizes containing

no more than 4,500 mg. Schedule III if over

4,500 mg

Unscheduled for adult use. In package sizes containing

no more than 4,500 mg. Schedule III if over

4,500 mg

Unscheduled for adult use. In package sizes containing

no more than 4,500 mg. Schedule III if over

4,500 mg

Unscheduled for adult use. In package sizes containing

no more than 4,500 mg. Schedule III if over

4,500 mg

Unscheduled for adult use. In package sizes containing

no more than 4,500 mg. Schedule III if over

4,500 mg

Product Catalog

Pharmascience Inc., 6111, Royalmount Avenue, Suite 100, Montréal (QC), Canada H4P 2T4 2

Zantac is a registered trademark of GlaxoSmithKline

Strength DIN/NPN Format National Brand Reference Shelf Life

75 mg 02247551Blistered 10 countBlistered 30 count Blistered 60 count

24 Months

Medicinal Ingredient Non-Medicinal Ingredients

ACTIVE INGREDIENTS: Each tablet contains: 75 mg of Ranitidine,

as Ranitidine Hydrochloride.

Colloidal Silicon Dioxide, Iron Oxide Red, Magnesium Stearate, Microcrystalline Cellulose, Polyvinyl Alcohol, Sodium Croscarmellose, Soy Lecithin,

Talc, Titanium Dioxide, Xanthan Gum

Unscheduled in package sizes containing no more than 4,500 mg. Schedule

III if over 4,500 mg.

Unscheduled in package sizes containing no more than 4,500 mg. Schedule

III if over 4,500 mg.

Unscheduled in package sizes containing no more than 4,500 mg. Schedule

III if over 4,500 mg.

Unscheduled in package sizes containing no more than 4,500 mg. Schedule

III if over 4,500 mg.

Unscheduled in package sizes containing no more than 4,500 mg. Schedule

III if over 4,500 mg.

Unscheduled in package sizes containing no more than 4,500 mg. Schedule

III if over 4,500 mg.

Annexe 3

Unscheduled in package sizes containing no more than 4,500 mg. Schedule

III if over 4,500 mg.

Unscheduled in package sizes containing no more than 4,500 mg. Schedule

III if over 4,500 mg.

Unscheduled in package sizes containing no more than 4,500 mg. Schedule

III if over 4,500 mg.

Unscheduled in package sizes containing no more than 4,500 mg. Schedule

III if over 4,500 mg.

Unscheduled in package sizes containing no more than 4,500 mg. Schedule

III if over 4,500 mg.

Ranitidine 75 mg

ZANTAC®

NWT (Follows Napra National)

BC Alberta Manitoba (Follows Napra National)

Saskatchewan (Follows Napra National)

Ontario (Follows Napra National)

Quebec New Brunswick (Follows Napra National)

PEI (Follows Napra National)

Nova Scotia (Follows Napra National)

Nfld Yukon (Follows Napra National)

Product Catalog

Naproxen Sodium 220mg

Pharmascience Inc., 6111, Royalmount Avenue, Suite 100, Montréal (QC), Canada H4P 2T4 3

ALEVE®

Aleve is a registered trademark of Bayer

Strength DIN/NPN Format National Brand Reference Shelf Life

220 mg 02362430

Bottled 24 countBottled 50 countBottled 100 countBottled 200 count

24 Months

Medicinal Ingredient Non-Medicinal Ingredients

ACTIVE INGREDIENTS: Each tablet contains:

220 mg Naproxen Sodium.

FD&C Blue No.2 Aluminum Lake, Hypromellose, Maize Starch, MicrocrystallineCellulose, Polyethylene Glycol, Povidone, Sodium Starch Glycolate, Stearic Acid,

Titanium Dioxide

When sold in products labeled with a recommended max daily dose of 440 mg:

Unscheduled for adult use. In package sizes of up to 6,600 mg. Schedule III in package sizes exceeding 6,600 mg

When sold in products labeled with a recommended max daily dose of 440 mg:

Unscheduled for adult use. In package sizes of up to 6,600 mg. Schedule III in package sizes exceeding 6,600 mg

When sold in products labeled with a recommended max daily dose of 440 mg:

Unscheduled for adult use. In package sizes of up to 6,600 mg. Schedule III in package sizes exceeding 6,600 mg

When sold in products labeled with a recommended max daily dose of 440 mg:

Unscheduled for adult use. In package sizes of up to 6,600 mg. Schedule III in package sizes exceeding 6,600 mg

When sold in products labeled with a recommended max daily dose of 440 mg:

Unscheduled for adult use. In package sizes of up to 6,600 mg. Schedule III in package sizes exceeding 6,600 mg

When sold in products labeled with a recommended max daily dose of 440 mg:

Unscheduled for adult use. In package sizes of up to 6,600 mg. Schedule III in package sizes exceeding 6,600 mg

Annexe 2

When sold in products labeled with a recommended max daily dose of 440 mg:

Unscheduled for adult use. In package sizes of up to 6,600 mg. Schedule III in package sizes exceeding 6,600 mg

When sold in products labeled with a recommended max daily dose of 440 mg:

Unscheduled for adult use. In package sizes of up to 6,600 mg. Schedule III in package sizes exceeding 6,600 mg

When sold in products labeled with a recommended max daily dose of 440 mg:

Unscheduled for adult use. In package sizes of up to 6,600 mg. Schedule III in package sizes exceeding 6,600 mg

When sold in products labeled with a recommended max daily dose of 440 mg: Schedule III in package sizes of up to 6,600 mg.

Schedule II in package sizes exceeding 6,600 mg

When sold in products labeled with a recommended max daily dose of 440 mg: Schedule III in package sizes of up to 6,600 mg.

Schedule II in package sizes exceeding 6,600 mg

NWT (Follows Napra National)

BC Alberta Manitoba (Follows Napra National)

Saskatchewan (Follows Napra National)

Ontario (Follows Napra National)

Quebec New Brunswick (Follows Napra National)

PEI (Follows Napra National)

Nova Scotia (Follows Napra National)

Nfld Yukon (Follows Napra National)

Product Catalog

Pharmascience Inc., 6111, Royalmount Avenue, Suite 100, Montréal (QC), Canada H4P 2T4 4

Imodium is a registered trademark of McNeil consumer healthcare a division of Johnson & Johnson

Strength DIN/NPN Format National Brand Reference Shelf Life

2 mg 02248994

Blistered 6 count Blistered 12 count Blistered 24 count Blistered 42 count

48 Months

Medicinal Ingredient Non-Medicinal Ingredients

ACTIVE INGREDIENTS: Each tablet contains:

2 mg Loperamide hydrochloride.

Croscarmellose Sodium, D&C Yellow No. 10 Aluminum Lake,

FD&C Blue No. 1 Aluminum Lake, Lactose, Magnesium Stearate, Microcrystalline Cellulose and Povidone

Unscheduled for adult use.

Unscheduled for adult use.

Unscheduled for adult use.

Unscheduled for adult use.

Unscheduled for adult use.

Unscheduled for adult use.

Annexe 3Unscheduled for adult use.

Unscheduled for adult use.

Unscheduled for adult use.

Unscheduled for adult use.

Unscheduled for adult use.

Loperamide hydrochloride 2 mg

IMODIUM®

NWT (Follows Napra National)

BC Alberta Manitoba (Follows Napra National)

Saskatchewan (Follows Napra National)

Ontario (Follows Napra National)

Quebec New Brunswick (Follows Napra National)

PEI (Follows Napra National)

Nova Scotia (Follows Napra National)

Nfld Yukon (Follows Napra National)

Product Catalog

Pharmascience Inc., 6111, Royalmount Avenue, Suite 100, Montréal (QC), Canada H4P 2T4 5

Aerius is a registered trademark of Schering

Strength DIN/NPN Format National Brand Reference Shelf Life

5 mg 02298155

Blistered 10 count Blistered 20 count Blistered 30 count Blistered 50 count

36 Months

Medicinal Ingredient Non-Medicinal Ingredients

ACTIVE INGREDIENTS: Each tablet contains: Desloratadine 5 mg.

FD&C Blue No. 2 Aluminum Lake, Hydroxypropyl Methylcellulose, Lactose,

Magnesium Oxide, Microcrystalline Cellulose, Polyethylene Glycol, Pregelatinized Corn Starch, Titanium Dioxide, Zinc Stearate

Unscheduled for adult use.

Unscheduled for adult use.

Unscheduled for adult use.

Unscheduled for adult use.

Unscheduled for adult use.

Unscheduled for adult use.

Annexe 3Unscheduled for adult use.

Unscheduled for adult use.

Unscheduled for adult use.

Unscheduled for adult use.

Unscheduled for adult use.

Desloratadine 5 mg

AERIUS®

NWT (Follows Napra National)

BC Alberta Manitoba (Follows Napra National)

Saskatchewan (Follows Napra National)

Ontario (Follows Napra National)

Quebec New Brunswick (Follows Napra National)

PEI (Follows Napra National)

Nova Scotia (Follows Napra National)

Nfld Yukon (Follows Napra National)

Product Catalog

Pharmascience Inc., 6111, Royalmount Avenue, Suite 100, Montréal (QC), Canada H4P 2T4 6

Reactine is a registered trademark of Pfizer

Strength DIN/NPN Format National Brand Reference Shelf Life

10 mg 02315955Blistered 20 count Blistered 30 count

24 Months

Medicinal Ingredient Non-Medicinal Ingredients

ACTIVE INGREDIENTS: Each tablet contains:

10 mg of Cetirizine Hydrochloride.

Corn Starch, Hydroxypropyl Methylcellulose, Lactose, Magnesium Stearate,

Polyethylene Glycol, Povidone, Titanium Dioxide

Unscheduled in concentrations of 10 mg equivalent to 8.5 mg or

less of cetirizine base per dosage unit in products marketed for adult use.

Unscheduled for adult use.

Unscheduled in concentrations of 10 mg equivalent to 8.5 mg or

less of cetirizine base per dosage unit in products marketed for adult use.

Unscheduled in concentrations of 10 mg equivalent to 8.5 mg or

less of cetirizine base per dosage unit in products marketed for adult use.

Unscheduled in concentrations of 10 mg equivalent to 8.5 mg or

less of cetirizine base per dosage unit in products marketed for adult use.

Unscheduled in concentrations of 10 mg equivalent to 8.5 mg or

less of cetirizine base per dosage unit in products marketed for adult use.

Annexe 3

Unscheduled in concentrations of 10 mg equivalent to 8.5 mg or

less of cetirizine base per dosage unit in products marketed for adult use.

Unscheduled in concentrations of 10 mg equivalent to 8.5 mg or

less of cetirizine base per dosage unit in products marketed for adult use.

Unscheduled in concentrations of 10 mg equivalent to 8.5 mg or

less of cetirizine base per dosage unit in products marketed for adult use.

Unscheduled in concentrations of 10 mg equivalent to 8.5 mg or

less of cetirizine base per dosage unit in products marketed for adult use.

Unscheduled in concentrations of 10 mg equivalent to 8.5 mg or

less of cetirizine base per dosage unit in products marketed for adult use.

Cetirizine Hydrochloride 10 mg

REACTINE®

NWT (Follows Napra National)

BC Alberta Manitoba (Follows Napra National)

Saskatchewan (Follows Napra National)

Ontario (Follows Napra National)

Quebec New Brunswick (Follows Napra National)

PEI (Follows Napra National)

Nova Scotia (Follows Napra National)

Nfld Yukon (Follows Napra National)

Product Catalog

Pharmascience Inc., 6111, Royalmount Avenue, Suite 100, Montréal (QC), Canada H4P 2T4 7

Aspirin is a registered trademark of Bayer

Strength DIN/NPN Format National Brand Reference Shelf Life

81 mg 02244993Bottled 30 count Bottled 120 countBottled 180 count

36 Months

Medicinal Ingredient Non-Medicinal Ingredients

ACTIVE INGREDIENTS: Each tablet contains:

Acetylsalicylic acid 81 mg.

Colloidal Silicon Dioxide, Lactose Anhydrous, Methacrylic Acid Copolymer Type C, Methylated Silica, Methylcellulose, Polydimethylsiloxane, Polyethylene Glycol,

Pregelatinized Starch, Purified Water, Sodium Bicarbonate, Sodium Lauryl Sulphate, Sorbitan Tristearate, Stearic Acid, Talc, Titanium Dioxide, Triethyl Citrate

III (in products intended for oral adult use in

strengths of 81 mg per dosage unit and 650 mg

or greater per dosage unit, and in rectal preparations containing more than 150

mg per dosage unit)

III (in products intended for oral adult use in

strengths of 81 mg per dosage unit and 650 mg

or greater per dosage unit, and in rectal preparations containing more than 150

mg per dosage unit)

Unscheduled (over 80 mg)

III (in products intended for oral adult use in

strengths of 81 mg per dosage unit and 650 mg

or greater per dosage unit, and in rectal preparations containing more than 150

mg per dosage unit)

III (in products intended for oral adult use in

strengths of 81 mg per dosage unit and 650 mg

or greater per dosage unit, and in rectal preparations containing more than 150

mg per dosage unit)

III (in products intended for oral adult use in

strengths of 81 mg per dosage unit and 650 mg

or greater per dosage unit, and in rectal preparations containing more than 150

mg per dosage unit)

Annexe 3 for over 30 tabs, hors annexe 30 or less

III (in products intended for oral adult use in

strengths of 81 mg per dosage unit and 650 mg

or greater per dosage unit, and in rectal preparations containing more than 150

mg per dosage unit)

III (in products intended for oral adult use in

strengths of 81 mg per dosage unit and 650 mg

or greater per dosage unit, and in rectal preparations containing more than 150

mg per dosage unit)

III (in products intended for oral adult use in

strengths of 81 mg per dosage unit and 650 mg

or greater per dosage unit, and in rectal preparations containing more than 150

mg per dosage unit)

III (in products intended for oral adult use in

strengths of 81 mg per dosage unit and 650 mg

or greater per dosage unit, and in rectal preparations containing more than 150

mg per dosage unit)

III (in products intended for oral adult use in

strengths of 81 mg per dosage unit and 650 mg

or greater per dosage unit, and in rectal preparations containing more than 150

mg per dosage unit)

ASA 81mg EC

ASPIRIN®

NWT (Follows Napra National)

BC Alberta Manitoba (Follows Napra National)

Saskatchewan (Follows Napra National)

Ontario (Follows Napra National)

Quebec New Brunswick (Follows Napra National)

PEI (Follows Napra National)

Nova Scotia (Follows Napra National)

Nfld Yukon (Follows Napra National)

Product Catalog

Pharmascience Inc., 6111, Royalmount Avenue, Suite 100, Montréal (QC), Canada H4P 2T4 8

Aspirin is a registered trademark of Bayer

Strength DIN/NPN Format National Brand Reference Shelf Life

81 mg 02304651Bottled 120 countBottled 180 count

36 Months

Medicinal Ingredient Non-Medicinal Ingredients

ACTIVE INGREDIENTS: Each tablet contains:

Acetylsalicylic acid 81mg.

D&C Yellow No. 10, FD&C Red No. 40, Mannitol, Orange Flavour, Pregelatinized Starch, Sodium Saccharin, Stearic Acid

III (in products intended for oral adult use in

strengths of 81 mg per dosage unit and 650 mg

or greater per dosage unit, and in rectal preparations containing more than 150

mg per dosage unit)

III (in products intended for oral adult use in

strengths of 81 mg per dosage unit and 650 mg

or greater per dosage unit, and in rectal preparations containing more than 150

mg per dosage unit)

Unscheduled (over 80 mg)

III (in products intended for oral adult use in

strengths of 81 mg per dosage unit and 650 mg

or greater per dosage unit, and in rectal preparations containing more than 150

mg per dosage unit)

III (in products intended for oral adult use in

strengths of 81 mg per dosage unit and 650 mg

or greater per dosage unit, and in rectal preparations containing more than 150

mg per dosage unit)

III (in products intended for oral adult use in

strengths of 81 mg per dosage unit and 650 mg

or greater per dosage unit, and in rectal preparations containing more than 150

mg per dosage unit)

Annexe 3 for over 30 tabs, hors annexe 30 or less

III (in products intended for oral adult use in

strengths of 81 mg per dosage unit and 650 mg

or greater per dosage unit, and in rectal preparations containing more than 150

mg per dosage unit)

III (in products intended for oral adult use in

strengths of 81 mg per dosage unit and 650 mg

or greater per dosage unit, and in rectal preparations containing more than 150

mg per dosage unit)

III (in products intended for oral adult use in

strengths of 81 mg per dosage unit and 650 mg

or greater per dosage unit, and in rectal preparations containing more than 150

mg per dosage unit)

III (in products intended for oral adult use in

strengths of 81 mg per dosage unit and 650 mg

or greater per dosage unit, and in rectal preparations containing more than 150

mg per dosage unit)

III (in products intended for oral adult use in

strengths of 81 mg per dosage unit and 650 mg

or greater per dosage unit, and in rectal preparations containing more than 150

mg per dosage unit)

ASA 81mg Chew

ASPIRIN®

NWT (Follows Napra National)

BC Alberta Manitoba (Follows Napra National)

Saskatchewan (Follows Napra National)

Ontario (Follows Napra National)

Quebec New Brunswick (Follows Napra National)

PEI (Follows Napra National)

Nova Scotia (Follows Napra National)

Nfld Yukon (Follows Napra National)

Product Catalog

Pharmascience Inc., 6111, Royalmount Avenue, Suite 100, Montréal (QC), Canada H4P 2T4 9

Advil is a registered trademark of Pfizer

Strength DIN/NPN Format National Brand Reference Shelf Life

200 mg 02314762Bottled 30 countBottled 60 count Bottled 120 count

48 Months

Medicinal Ingredient Non-Medicinal Ingredients

ACTIVE INGREDIENTS: Each tablet contains: 200 mg of Ibuprofen.

Colloidal Sillicon Dioxide, Corn Starch, Dextrose Monohydrate, Hypromellose, Iron Oxide Red, Lactose Monohydrate, Lecithin, Maltodextrin, Povidone,

Pregelatinized Starch, Sodium Carboxymethylcellulose, Sodium Starch Glycolate, Stearic Acid, Titanium Dioxide, Triacetin

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in

package sizes of up to 18,000 mg) Unscheduled

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in package sizes exceeding

18,000 mg) Schedule

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in

package sizes of up to 18,000 mg) Unscheduled

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in package sizes exceeding

18,000 mg) Schedule

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in

package sizes of up to 18,000 mg) Unscheduled

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in package sizes exceeding

18,000 mg) Schedule

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in

package sizes of up to 18,000 mg) Unscheduled

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in package sizes exceeding

18,000 mg) Schedule

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in

package sizes of up to 18,000 mg) Unscheduled

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in package sizes exceeding

18,000 mg) Schedule

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in

package sizes of up to 18,000 mg) Unscheduled

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in package sizes exceeding

18,000 mg) Schedule

Annexe 3 (less than 400mg)

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in

package sizes of up to 18,000 mg) Unscheduled

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in package sizes exceeding

18,000 mg) Schedule

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in

package sizes of up to 18,000 mg) Unscheduled

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in package sizes exceeding

18,000 mg) Schedule

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in

package sizes of up to 18,000 mg) Unscheduled

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in package sizes exceeding

18,000 mg) Schedule

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in

package sizes of up to 18,000 mg) Unscheduled

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in package sizes exceeding

18,000 mg) Schedule

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in

package sizes of up to 18,000 mg) Unscheduled

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in package sizes exceeding

18,000 mg) Schedule

Ibuprofen 200 mg

ADVIL®

NWT (Follows Napra National)

BC Alberta Manitoba (Follows Napra National)

Saskatchewan (Follows Napra National)

Ontario (Follows Napra National)

Quebec New Brunswick (Follows Napra National)

PEI (Follows Napra National)

Nova Scotia (Follows Napra National)

Nfld Yukon (Follows Napra National)

Product Catalog

Pharmascience Inc., 6111, Royalmount Avenue, Suite 100, Montréal (QC), Canada H4P 2T4 10

Advil is a registered trademark of Pfizer

Strength DIN/NPN Format National Brand Reference Shelf Life

400 mg 02314770Bottled 32 countBottled 72 count

48 Months

Medicinal Ingredient Non-Medicinal Ingredients

ACTIVE INGREDIENTS: Each tablet contains: 400 mg of Ibuprofen.

Colloidal Sillicon Dioxide, Corn Starch, Dextrose Monohydrate, Hypromellose, Iron Oxide Red, Lactose Monohydrate, Lecithin, Maltodextrin, Povidone,

Pregelatinized Starch, Sodium Carboxymethylcellulose, Sodium Starch Glycolate, Stearic Acid, Titanium Dioxide, Triacetin

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in

package sizes of up to 18,000 mg) Unscheduled

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in package sizes exceeding

18,000 mg) Schedule

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in

package sizes of up to 18,000 mg) Unscheduled

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in package sizes exceeding

18,000 mg) Schedule

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in

package sizes of up to 18,000 mg) Unscheduled

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in package sizes exceeding

18,000 mg) Schedule

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in

package sizes of up to 18,000 mg) Unscheduled

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in package sizes exceeding

18,000 mg) Schedule

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in

package sizes of up to 18,000 mg) Unscheduled

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in package sizes exceeding

18,000 mg) Schedule

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in

package sizes of up to 18,000 mg) Unscheduled

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in package sizes exceeding

18,000 mg) Schedule

Annexe 2

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in

package sizes of up to 18,000 mg) Unscheduled

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in package sizes exceeding

18,000 mg) Schedule

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in

package sizes of up to 18,000 mg) Unscheduled

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in package sizes exceeding

18,000 mg) Schedule

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in

package sizes of up to 18,000 mg) Unscheduled

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in package sizes exceeding

18,000 mg) Schedule

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in

package sizes of up to 18,000 mg) Unscheduled

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in package sizes exceeding

18,000 mg) Schedule

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in

package sizes of up to 18,000 mg) Unscheduled

Ibuprofen and its salts containing 400 mg or less per oral dosage unit (when sold in package sizes exceeding

18,000 mg) Schedule

Ibuprofen 400 mg

ADVIL®

NWT (Follows Napra National)

BC Alberta Manitoba (Follows Napra National)

Saskatchewan (Follows Napra National)

Ontario (Follows Napra National)

Quebec New Brunswick (Follows Napra National)

PEI (Follows Napra National)

Nova Scotia (Follows Napra National)

Nfld Yukon (Follows Napra National)

Product Catalog

Pharmascience Inc., 6111, Royalmount Avenue, Suite 100, Montréal (QC), Canada H4P 2T4 11

Colace is a registered trademark of Wellspring Pharmaceutical Canada corporation

Strength DIN/NPN Format National Brand Reference Shelf Life

100 mg 02281031 Bottled 100 count 24 Months

Medicinal Ingredient Non-Medicinal Ingredients

ACTIVE INGREDIENTS: Each capsule contains:

100 mg of Docusate Sodium.

FD&C Red No. 40, FD&C Yellow No. 6, Gelatin, Glycerin, Polyethylene Glycol, Propylene Glycol, Sodium methylparaben, sodium Propylparaben, Purified Water, Sorbitol.

Unscheduled Unscheduled Unscheduled Unscheduled Unscheduled Unscheduled

Unscheduled Unscheduled Unscheduled. Unscheduled Unscheduled Unscheduled

Docusate Sodium 100 mg

COLACE®

NWT (Follows Napra National)

BC Alberta Manitoba (Follows Napra National)

Saskatchewan (Follows Napra National)

Ontario (Follows Napra National)

Quebec New Brunswick (Follows Napra National)

PEI (Follows Napra National)

Nova Scotia (Follows Napra National)

Nfld Yukon (Follows Napra National)