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Propranolol Hydrochloride - 50111-471-01 - (Propranolol Hydrochloride)

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Drug Information of Propranolol Hydrochloride

Product NDC: 50111-471
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: 50111-471
Labeler Name: Pliva Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071976
Marketing Category: ANDA
Start Marketing Date: 19900930

Package Information of Propranolol Hydrochloride

Package NDC: 50111-471-01
Package Description: 100 TABLET in 1 BOTTLE (50111-471-01)

NDC Information of Propranolol Hydrochloride

NDC Code 50111-471-01
Proprietary Name Propranolol Hydrochloride
Package Description 100 TABLET in 1 BOTTLE (50111-471-01)
Product NDC 50111-471
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Propranolol Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19900930
Marketing Category Name ANDA
Labeler Name Pliva Inc.
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


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