Home > National Drug Code (NDC) > Ranitidine Hydrochloride

Ranitidine Hydrochloride - 68094-204-61 - (Ranitidine Hydrochloride)

Alphabetical Index


Drug Information of Ranitidine Hydrochloride

Product NDC: 68094-204
Proprietary Name: Ranitidine Hydrochloride
Non Proprietary Name: Ranitidine Hydrochloride
Active Ingredient(s): 150    mg/10mL & nbsp;   Ranitidine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ranitidine Hydrochloride

Product NDC: 68094-204
Labeler Name: Precision Dose Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078312
Marketing Category: ANDA
Start Marketing Date: 20030821

Package Information of Ranitidine Hydrochloride

Package NDC: 68094-204-61
Package Description: 10 TRAY in 1 CASE (68094-204-61) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE (68094-204-59)

NDC Information of Ranitidine Hydrochloride

NDC Code 68094-204-61
Proprietary Name Ranitidine Hydrochloride
Package Description 10 TRAY in 1 CASE (68094-204-61) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE (68094-204-59)
Product NDC 68094-204
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ranitidine Hydrochloride
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20030821
Marketing Category Name ANDA
Labeler Name Precision Dose Inc.
Substance Name RANITIDINE HYDROCHLORIDE
Strength Number 150
Strength Unit mg/10mL
Pharmaceutical Classes Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

Complete Information of Ranitidine Hydrochloride


General Information