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Propranolol Hydrochloride - 63629-2570-4 - (Propranolol Hydrochloride)

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Drug Information of Propranolol Hydrochloride

Product NDC: 63629-2570
Proprietary Name: Propranolol Hydrochloride
Non Proprietary Name: Propranolol Hydrochloride
Active Ingredient(s): 20    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: 63629-2570
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078955
Marketing Category: ANDA
Start Marketing Date: 20081013

Package Information of Propranolol Hydrochloride

Package NDC: 63629-2570-4
Package Description: 60 TABLET in 1 BOTTLE (63629-2570-4)

NDC Information of Propranolol Hydrochloride

NDC Code 63629-2570-4
Proprietary Name Propranolol Hydrochloride
Package Description 60 TABLET in 1 BOTTLE (63629-2570-4)
Product NDC 63629-2570
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Propranolol Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20081013
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name PROPRANOLOL HYDROCHLORIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Propranolol Hydrochloride


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