Zantac 75 - 0597-0122-08 - (ranitidine)

Alphabetical Index


Drug Information of Zantac 75

Product NDC: 0597-0122
Proprietary Name: Zantac 75
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 Zantac 75

Product NDC: 0597-0122
Labeler Name: Boehringer Ingelheim Pharmaceuticals Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA020520
Marketing Category: NDA
Start Marketing Date: 20061221

Package Information of Zantac 75

Package NDC: 0597-0122-08
Package Description: 1 TABLET, COATED in 1 POUCH (0597-0122-08)

NDC Information of Zantac 75

NDC Code 0597-0122-08
Proprietary Name Zantac 75
Package Description 1 TABLET, COATED in 1 POUCH (0597-0122-08)
Product NDC 0597-0122
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ranitidine
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20061221
Marketing Category Name NDA
Labeler Name Boehringer Ingelheim Pharmaceuticals Inc.
Substance Name RANITIDINE HYDROCHLORIDE
Strength Number 75
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Zantac 75


General Information