NDC | 41167-0310-0, 41167-0310-1, 41167-0310-2, 41167-0310-3, 41167-0310-4, 41167-0310-5, 41167-0310-6, 41167-0310-7, 41167-0310-8, 41167-0310-9 |
Set ID | 78380bf5-7ab6-42da-a02c-24644db778ff |
Category | HUMAN OTC DRUG LABEL |
Packager | Chattem, Inc. |
Generic Name | |
Product Class | |
Product Number | |
Application Number | NDA021698 |
- SPL UNCLASSIFIED SECTION
- 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
- 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
- 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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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?
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ZANTAC 150 MAXIMUM STRENGTH
ranitidine hydrochloride tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41167-0310 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 HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) FERRIC OXIDE RED (UNII: 1K09F3G675) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) TRIACETIN (UNII: XHX3C3X673) Product Characteristics Color PINK (dark pink) Score no score Shape PENTAGON (5 SIDED) Size 4mm Flavor Imprint Code Z;150 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41167-0310-1 1 in 1 CARTON 10/12/2018 1 3 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:41167-0310-2 1 in 1 CARTON 08/17/2018 2 8 in 1 BLISTER PACK; Type 0: Not a Combination Product 3 NDC:41167-0310-3 3 in 1 CARTON 08/17/2018 3 8 in 1 BLISTER PACK; Type 0: Not a Combination Product 4 NDC:41167-0310-7 1 in 1 CARTON 04/03/2018 4 40 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 5 NDC:41167-0310-4 1 in 1 CARTON 04/03/2018 5 50 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 6 NDC:41167-0310-5 1 in 1 CARTON 04/03/2018 6 65 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 7 NDC:41167-0310-8 2 in 1 CARTON 04/03/2018 7 60 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 8 NDC:41167-0310-9 1 in 1 CARTON 04/03/2018 8 78 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 9 NDC:41167-0310-6 1 in 1 CARTON 04/03/2018 9 90 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10 NDC:41167-0310-0 1 in 1 CARTON 11/11/2018 10 1 in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA021698 04/03/2018 Labeler - Chattem, Inc. (003336013)