NDC | 55648-741-00, 55648-741-01, 55648-741-02, 55648-741-03, 55648-741-05, 55648-741-06 |
Set ID | d6cfdf6c-9b09-440e-81a4-04d45d247751 |
Category | HUMAN OTC DRUG LABEL |
Packager | WOCKHARDT LIMITED |
Generic Name | |
Product Class | |
Product Number | |
Application Number | ANDA078653 |
- Active ingredient (in each tablet)
- Purpose
- Uses
- Warnings
- Do not use
-
Ask a doctor before use if you have
- frequent chest pain
- frequent wheezing, particularly with heartburn
- unexplained weight loss
- nausea or vomiting
- stomach pain
- 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
- Stop use and ask a doctor if
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
-
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
Questions or comments?
Call 1-800-346-6854
Read the directions, consumer information leaflet and warnings before use. Keep the carton. It contains important information.
Manufactured by:
Wockhardt Limited,
Mumbai, India.
Distributed by:
Wockhardt USA LLC.
20 Waterview Blvd.
Parsippany, NJ 07054
USA.
Rev.151111 - PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
RANITIDINE
ranitidine tablet, coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55648-741 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 CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) MAGNESIUM STEARATE (UNII: 70097M6I30) COLLOIDAL SILICON DIOXIDE (UNII: ETJ7Z6XBU4) HYPROMELLOSES (UNII: 3NXW29V3WO) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) FERRIC OXIDE RED (UNII: 1K09F3G675) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) DIETHYL PHTHALATE (UNII: UF064M00AF) Product Characteristics Color orange (orange colored film coated) Score no score Shape HEXAGON (6 sided) Size 10mm Flavor Imprint Code W741 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55648-741-01 1 in 1 CARTON 1 10 in 1 BOTTLE 2 NDC:55648-741-02 1 in 1 CARTON 2 100 in 1 BOTTLE 3 NDC:55648-741-05 1 in 1 CARTON 3 500 in 1 BOTTLE 4 NDC:55648-741-03 10 in 1 CARTON 4 10 in 1 BLISTER PACK 5 NDC:55648-741-06 6000 in 1 POUCH 6 NDC:55648-741-00 30000 in 1 DRUM Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA078653 11/26/2007 Labeler - WOCKHARDT LIMITED (650069115) Establishment Name Address ID/FEI Business Operations WOCKHARDT LIMITED 676257570 manufacture