Label: WAL-ZAN- ranitidine hydrochloride tablets 150mg tablet, coated
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NDC Code(s):
0363-0010-01,
0363-0010-23,
0363-0010-26,
0363-0010-32, view more0363-0010-34, 0363-0010-50, 0363-0010-61, 0363-0010-62
- Packager: Walgreens Company
- This is a repackaged label.
- Source NDC Code(s): 55111-404
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated September 30, 2019
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient (in each tablet)
- Purpose
- Use(s)
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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
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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
- adults and children 12 years and over:
- Other information
- Inactive ingredients
- Questions
- container label
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INGREDIENTS AND APPEARANCE
WAL-ZAN
ranitidine hydrochloride tablets 150mg tablet, coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0010(NDC:55111-404) 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 FD&C RED NO. 40 (UNII: WZB9127XOA) HYPROMELLOSE 2910 (6 MPA.S) (UNII: 0WZ8WG20P6) FERROSOFERRIC OXIDE (UNII: XM0M87F357) magnesium stearate (UNII: 70097M6I30) cellulose, microcrystalline (UNII: OP1R32D61U) POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) titanium dioxide (UNII: 15FIX9V2JP) Product Characteristics Color PINK Score no score Shape ROUND Size 9mm Flavor Imprint Code R150 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-0010-34 1 in 1 CARTON 06/11/2011 09/30/2019 1 24 in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:0363-0010-50 1 in 1 CARTON 06/11/2011 09/30/2019 2 50 in 1 BOTTLE; Type 0: Not a Combination Product 3 NDC:0363-0010-62 1 in 1 CARTON 06/11/2011 09/30/2019 3 95 in 1 BOTTLE; Type 0: Not a Combination Product 4 NDC:0363-0010-32 1 in 1 CARTON 06/11/2011 09/30/2019 4 32 in 1 BOTTLE; Type 0: Not a Combination Product 5 NDC:0363-0010-01 1 in 1 CARTON 06/11/2011 09/30/2019 5 200 in 1 BOTTLE; Type 0: Not a Combination Product 6 NDC:0363-0010-23 1 in 1 CARTON 06/11/2011 09/30/2019 6 36 in 1 BOTTLE; Type 0: Not a Combination Product 7 NDC:0363-0010-26 1 in 1 CARTON 06/11/2011 09/30/2019 7 65 in 1 BOTTLE; Type 0: Not a Combination Product 8 NDC:0363-0010-61 1 in 1 CARTON 06/11/2011 09/30/2019 8 65 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 ANDA078192 06/11/2011 Labeler - Walgreens Company (008965063)