NDC | 0363-1030-01, 0363-1030-02, 0363-1030-05, 0363-1030-06, 0363-1030-07, 0363-1030-09 |
Set ID | de5b9882-5dd1-c49f-2602-cc69ce309e86 |
Category | HUMAN OTC DRUG LABEL |
Packager | Walgreens Company |
Generic Name | |
Product Class | |
Product Number | |
Application Number | ANDA200172 |
- Drug Facts 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 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
-
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 or comments?
- Principal Display Panel
-
INGREDIENTS AND APPEARANCE
WAL-ZAN
wal-zan tabletProduct 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)