Home > National Drug Code (NDC) > Propranolol Hydrochloride

Propranolol Hydrochloride - 63629-3587-2 - (Propranolol Hydrochloride)

Alphabetical Index


Drug Information of Propranolol Hydrochloride

Product NDC: 63629-3587
Proprietary Name: Propranolol Hydrochloride
Non Proprietary Name: Propranolol Hydrochloride
Active Ingredient(s): 80    mg/1 & nbsp;   Propranolol Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Propranolol Hydrochloride

Product NDC: 63629-3587
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070178
Marketing Category: ANDA
Start Marketing Date: 19860513

Package Information of Propranolol Hydrochloride

Package NDC: 63629-3587-2
Package Description: 100 TABLET in 1 BOTTLE (63629-3587-2)

NDC Information of Propranolol Hydrochloride

NDC Code 63629-3587-2
Proprietary Name Propranolol Hydrochloride
Package Description 100 TABLET in 1 BOTTLE (63629-3587-2)
Product NDC 63629-3587
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Propranolol Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19860513
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name PROPRANOLOL HYDROCHLORIDE
Strength Number 80
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Propranolol Hydrochloride


General Information