Ranitidine - 55111-131-04 - (Ranitidine)

Alphabetical Index


Drug Information of Ranitidine

Product NDC: 55111-131
Proprietary Name: Ranitidine
Non Proprietary Name: Ranitidine
Active Ingredient(s): 75    mg/1 & nbsp;   Ranitidine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Ranitidine

Product NDC: 55111-131
Labeler Name: Dr. Reddy's Laboratories Limited
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA075294
Marketing Category: ANDA
Start Marketing Date: 20000301

Package Information of Ranitidine

Package NDC: 55111-131-04
Package Description: 1 BOTTLE in 1 CARTON (55111-131-04) > 120 TABLET in 1 BOTTLE

NDC Information of Ranitidine

NDC Code 55111-131-04
Proprietary Name Ranitidine
Package Description 1 BOTTLE in 1 CARTON (55111-131-04) > 120 TABLET in 1 BOTTLE
Product NDC 55111-131
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ranitidine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20000301
Marketing Category Name ANDA
Labeler Name Dr. Reddy's Laboratories Limited
Substance Name RANITIDINE HYDROCHLORIDE
Strength Number 75
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Ranitidine


General Information