Home > National Drug Code (NDC) > Maximum Strength Zantac

Maximum Strength Zantac - 0597-0121-09 - (ranitidine)

Alphabetical Index


Drug Information of Maximum Strength Zantac

Product NDC: 0597-0121
Proprietary Name: Maximum Strength Zantac
Non Proprietary Name: ranitidine
Active Ingredient(s): 150    mg/1 & nbsp;   ranitidine
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Maximum Strength Zantac

Product NDC: 0597-0121
Labeler Name: Boehringer Ingelheim Pharmaceuticals Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA021698
Marketing Category: NDA
Start Marketing Date: 20061221

Package Information of Maximum Strength Zantac

Package NDC: 0597-0121-09
Package Description: 4 BLISTER PACK in 1 CARTON (0597-0121-09) > 8 TABLET, COATED in 1 BLISTER PACK

NDC Information of Maximum Strength Zantac

NDC Code 0597-0121-09
Proprietary Name Maximum Strength Zantac
Package Description 4 BLISTER PACK in 1 CARTON (0597-0121-09) > 8 TABLET, COATED in 1 BLISTER PACK
Product NDC 0597-0121
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 150
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Maximum Strength Zantac


General Information