Ranitidine - 50383-051-10 - (Ranitidine)

Alphabetical Index


Drug Information of Ranitidine

Product NDC: 50383-051
Proprietary Name: Ranitidine
Non Proprietary Name: Ranitidine
Active Ingredient(s): 16.8    mg/mL & nbsp;   Ranitidine
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ranitidine

Product NDC: 50383-051
Labeler Name: Hi-Tech Pharmacal Co., Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091078
Marketing Category: ANDA
Start Marketing Date: 20110322

Package Information of Ranitidine

Package NDC: 50383-051-10
Package Description: 10 CUP, UNIT-DOSE in 1 TRAY (50383-051-10) > 10 mL in 1 CUP, UNIT-DOSE

NDC Information of Ranitidine

NDC Code 50383-051-10
Proprietary Name Ranitidine
Package Description 10 CUP, UNIT-DOSE in 1 TRAY (50383-051-10) > 10 mL in 1 CUP, UNIT-DOSE
Product NDC 50383-051
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ranitidine
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20110322
Marketing Category Name ANDA
Labeler Name Hi-Tech Pharmacal Co., Inc.
Substance Name RANITIDINE HYDROCHLORIDE
Strength Number 16.8
Strength Unit mg/mL
Pharmaceutical Classes Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

Complete Information of Ranitidine


General Information