Label: WAL-ZAN- ranitidine tablet
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Contains inactivated NDC Code(s)
NDC Code(s): 0363-0362-02, 0363-0362-23, 0363-0362-50, 0363-0362-52, view more0363-0362-95 - Packager: Walgreen Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated January 13, 2015
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT (IN EACH TABLET)
- PURPOSE
- USES
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WARNINGS
Allergy alert: Do not use if you are allergic to ranitidine or other acid reducers
Do Not Use
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- 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
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- with other acid reducers
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- if you have kidney disease, except under the advice and supervision of a doctor
Ask a doctor before use if you have
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- frequent chest pain
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- frequent wheezing, particularly with heartburn
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- unexplained weight loss
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- nausea or vomiting
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- stomach pain
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- had heartburn over 3 months. This may be a sign of a more serious condition.
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- heartburn with lightheadedness, sweating or dizziness
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- chest pain or shoulder pain with shortness of breath; sweating; pain spreading to arms, neck or shoulders; or lightheadedness
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DIRECTIONS
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- adults and children 12 years and over:
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- to relieve symptoms, swallow 1 tablet with a glass of water
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- to prevent symptoms, swallow 1 tablet with a glass of water 30 to 60 minutes before eating food or drinking beverages that cause heartburn
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- can be used up to twice daily (do not take more than 2 tablets in 24 hours)
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- children under 12 years: ask a doctor
- OTHER INFORMATION
- INACTIVE INGREDIENTS
- QUESTIONS?
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PRINCIPAL DISPLAY PANEL
Well at Walgreens
WALGREENS PHARMACIST RECOMMENDED*
NDC 0363-0362-02
MAXIMUM STRENGTH
Wal-Zan® 150
Ranitidine Tablets, USP 150 mg/Acid Reducer
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- Prevents & relieves heartburn associated with acid indigestion & sour stomach
200 TABLETS
Compare to Zantac 150® active ingredient‡‡
DISTRIBUTED BY: WALGREEN CO.
5114247/ORG115-F
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INGREDIENTS AND APPEARANCE
WAL-ZAN
ranitidine tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0362 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 SILICON DIOXIDE (UNII: ETJ7Z6XBU4) CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) HYPROMELLOSES (UNII: 3NXW29V3WO) FERRIC OXIDE RED (UNII: 1K09F3G675) MAGNESIUM STEARATE (UNII: 70097M6I30) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A) TALC (UNII: 7SEV7J4R1U) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color pink Score no score Shape OVAL (Oval, Shaped) Size 12mm Flavor Imprint Code 9R Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-0362-23 1 in 1 CARTON 1 24 in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:0363-0362-50 1 in 1 CARTON 2 50 in 1 BOTTLE; Type 0: Not a Combination Product 3 NDC:0363-0362-95 1 in 1 CARTON 3 95 in 1 BOTTLE; Type 0: Not a Combination Product 4 NDC:0363-0362-52 1 in 1 BOTTLE 4 65 in 1 BOTTLE; Type 0: Not a Combination Product 5 NDC:0363-0362-02 1 in 1 CARTON 5 200 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 ANDA200536 06/28/2011 Labeler - Walgreen Company (008965063) Registrant - Ranbaxy Pharmaceuticals Inc (937890044) Establishment Name Address ID/FEI Business Operations Shasun Pharmaceuticals Limited 915786829 MANUFACTURE(0363-0362)