Wal-Zan by Walgreens Company / Apotex Inc. / Accucaps Industries Limited / Accucaps Industries Limited Strathroy / Legacy Pharmaceutical Packaging WAL-ZAN tablet

Wal-Zan by

Drug Labeling and Warnings

Wal-Zan by is a Otc medication manufactured, distributed, or labeled by Walgreens Company, Apotex Inc., Accucaps Industries Limited, Accucaps Industries Limited Strathroy, Legacy Pharmaceutical Packaging. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts Active ingredient (in each tablet)

Ranitidine 150 mg (as ranitidine hydrochloride, USP 168 mg)

Purpose

Acid reducer

Uses

• relieves heartburn associated with acid indigestion and sour stomach
• prevents heartburn associated with acid indigestion and sour stomach brought on by eating or drinking certain foods and beverages

Warnings

Allergy alert: Do not use if you are allergic to ranitidine or other acid reducers

Do not use

• if you have trouble or pain swallowing food, vomiting with blood, or bloody or black stools. These may be signs of a serious condition. See your doctor.
• with other acid reducers
• if you have kidney disease, except under the advice and supervision of a doctor

Ask a doctor before use if you have 

• had heartburn over 3 months. This may be a sign of a more serious condition.
• heartburn with lightheadedness, sweating or dizziness 
• chest pain or shoulder pain with shortness of breath; sweating; pain spreading to arms, neck or shoulders; or lightheadedness
• frequent chest pain
• frequent wheezing, particularly with heartburn
• unexplained weight loss
• nausea or vomiting
• stomach pain

Stop use and ask a doctor if

• your heartburn continues or worsens
• you need to take this product for more than 14 days 

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

• adults and children 12 years and over:
  • to relieve symptoms, swallow 1 tablet with a glass of water
  • to prevent symptoms, swallow 1 tablet with a glass of water 30 to 60 minutes before eating food or drinking beverages that cause heartburn
  • can be used up to twice daily (do not take more than 2 tablets in 24 hours)
• children under 12 years; ask a doctor

Other information

• do not use if printed foil under bottle cap is broken or torn
• store at 20°C to 25°C (68°F to 77°F)
• avoid excessive heat or humidity
• this product is sodium and sugar free

Inactive ingredients

carnauba wax, colloidal silicon dioxide, ferric oxide red, ferric oxide yellow, hypromellose, magnesium stearate, microcrystalline cellulose, polydextrose, titanium dioxide and vanillin.

Questions or comments?

1-800-706-5575

Walgreens Pharmacist Recommended

Walgreens Pharmacist Survey

†† This product is not manufactured or distributed by Chattem [A Sanofi Company], distributor of ZANTAC 150Tablets. ZANTAC 150 is a registered trademark of Chattem [A Sanofi Company] 

Principal Display Panel

Walgreens

Maximum Strength

Wal-Zan® 150mg

Ranitidine Tablets, USP

150 mg/ Acid Reducer

24 Tablets

NDC: 0363-1030-02

INGREDIENTS AND APPEARANCE

WAL-ZAN 
wal-zan tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-1030
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RANITIDINE HYDROCHLORIDE (UNII: BK76465IHM) (RANITIDINE - UNII:884KT10YB7)	RANITIDINE	150 mg

Inactive Ingredients
Ingredient Name	Strength
CARNAUBA WAX (UNII: R12CBM0EIZ)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
HYPROMELLOSES (UNII: 3NXW29V3WO)
MAGNESIUM STEARATE (UNII: 70097M6I30)
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
POLYDEXTROSE (UNII: VH2XOU12IE)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
FERRIC OXIDE RED (UNII: 1K09F3G675)
VANILLIN (UNII: CHI530446X)

Product Characteristics
Color	PINK	Score	no score
Shape	ROUND	Size	9mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-1030-02	1 in 1 CARTON	07/31/2015
1		24 in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 0363-1030-05	1 in 1 CARTON	07/31/2015
2		50 in 1 BOTTLE; Type 0: Not a Combination Product
3	NDC: 0363-1030-09	1 in 1 CARTON	07/31/2015
3		95 in 1 BOTTLE; Type 0: Not a Combination Product
4	NDC: 0363-1030-06	1 in 1 CARTON	07/31/2015
4		65 in 1 BOTTLE; Type 0: Not a Combination Product
5	NDC: 0363-1030-01	1 in 1 CARTON	07/31/2015
5		65 in 1 BOTTLE; Type 0: Not a Combination Product
6	NDC: 0363-1030-07	1 in 1 CARTON	05/25/2017
6		200 in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA200172	07/31/2015

Labeler - Walgreens Company (008965063)

Registrant - Apotex Inc. (209429182)

Establishment
Name	Address	ID/FEI	Business Operations
Accucaps Industries Limited		248441727	analysis(0363-1030) , manufacture(0363-1030)

Establishment
Name	Address	ID/FEI	Business Operations
Accucaps Industries Limited Strathroy		243944050	analysis(0363-1030) , manufacture(0363-1030)

Establishment
Name	Address	ID/FEI	Business Operations
Legacy Pharmaceutical Packaging		143213275	pack(0363-1030)

Establishment
Name	Address	ID/FEI	Business Operations
Apotex Inc.		209429182	analysis(0363-1030) , manufacture(0363-1030)

Establishment
Name	Address	ID/FEI	Business Operations
Apotex Inc.		205576023	analysis(0363-1030) , manufacture(0363-1030)