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Propranolol Hydrochloride - 54868-0696-1 - (Propranolol Hydrochloride)

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Drug Information of Propranolol Hydrochloride

Product NDC: 54868-0696
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: 54868-0696
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078955
Marketing Category: ANDA
Start Marketing Date: 19950818

Package Information of Propranolol Hydrochloride

Package NDC: 54868-0696-1
Package Description: 30 TABLET in 1 BOTTLE (54868-0696-1)

NDC Information of Propranolol Hydrochloride

NDC Code 54868-0696-1
Proprietary Name Propranolol Hydrochloride
Package Description 30 TABLET in 1 BOTTLE (54868-0696-1)
Product NDC 54868-0696
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Propranolol Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19950818
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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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