NDC | 49035-404-13, 49035-404-34, 49035-404-61, 49035-404-65 |
Set ID | 83fd081b-30ae-68b4-5153-20d83caca0c1 |
Category | HUMAN OTC DRUG LABEL |
Packager | Walmart Stores Inc. |
Generic Name | |
Product Class | |
Product Number | |
Application Number | ANDA078192 |
- Active ingredient (in each tablet)
- Purpose
- Uses
-
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 diziness
- 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
- Ranitidine Tablets, 150 mg 24 count Carton
- Ranitidine Tablets, 150 mg 24 count Bottle
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INGREDIENTS AND APPEARANCE
RANITIDINE 150
ranitidine hydrochloride tablets 150mg tablet, coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49035-404(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:49035-404-34 1 in 1 CARTON 01/05/2010 1 24 in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:49035-404-61 1 in 1 CARTON 01/05/2010 2 65 in 1 BOTTLE; Type 0: Not a Combination Product 3 NDC:49035-404-13 2 in 1 CARTON 06/08/2018 3 65 in 1 BOTTLE; Type 0: Not a Combination Product 4 NDC:49035-404-65 1 in 1 CARTON 01/05/2010 4 220 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 01/05/2010 Labeler - Walmart Stores Inc. (051957769)