RANITIDINE - 64679-740-01 - (RANITIDINE)

Alphabetical Index


Drug Information of RANITIDINE

Product NDC: 64679-740
Proprietary Name: RANITIDINE
Non Proprietary Name: RANITIDINE
Active Ingredient(s): 75    mg/1 & nbsp;   RANITIDINE
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of RANITIDINE

Product NDC: 64679-740
Labeler Name: WOCKHARDT USA LLC.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA078884
Marketing Category: ANDA
Start Marketing Date: 20080731

Package Information of RANITIDINE

Package NDC: 64679-740-01
Package Description: 1 BOTTLE in 1 CARTON (64679-740-01) > 10 TABLET, COATED in 1 BOTTLE

NDC Information of RANITIDINE

NDC Code 64679-740-01
Proprietary Name RANITIDINE
Package Description 1 BOTTLE in 1 CARTON (64679-740-01) > 10 TABLET, COATED in 1 BOTTLE
Product NDC 64679-740
Product Type Name HUMAN OTC DRUG
Non Proprietary Name RANITIDINE
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20080731
Marketing Category Name ANDA
Labeler Name WOCKHARDT USA LLC.
Substance Name RANITIDINE HYDROCHLORIDE
Strength Number 75
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of RANITIDINE


General Information