RANITIDINE - 64679-694-01 - (RANITIDINE HYDROCHLORIDE)

Alphabetical Index


Drug Information of RANITIDINE

Product NDC: 64679-694
Proprietary Name: RANITIDINE
Non Proprietary Name: RANITIDINE HYDROCHLORIDE
Active Ingredient(s): 15    mg/mL & nbsp;   RANITIDINE HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): SYRUP
Coding System: National Drug Codes(NDC)

Labeler Information of RANITIDINE

Product NDC: 64679-694
Labeler Name: WOCKHARDT USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079211
Marketing Category: ANDA
Start Marketing Date: 20090526

Package Information of RANITIDINE

Package NDC: 64679-694-01
Package Description: 473 mL in 1 BOTTLE (64679-694-01)

NDC Information of RANITIDINE

NDC Code 64679-694-01
Proprietary Name RANITIDINE
Package Description 473 mL in 1 BOTTLE (64679-694-01)
Product NDC 64679-694
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name RANITIDINE HYDROCHLORIDE
Dosage Form Name SYRUP
Route Name ORAL
Start Marketing Date 20090526
Marketing Category Name ANDA
Labeler Name WOCKHARDT USA LLC
Substance Name RANITIDINE HYDROCHLORIDE
Strength Number 15
Strength Unit mg/mL
Pharmaceutical Classes Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

Complete Information of RANITIDINE


General Information