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Propranolol Hydrochloride - 54868-1517-2 - (Propranolol)

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Drug Information of Propranolol Hydrochloride

Product NDC: 54868-1517
Proprietary Name: Propranolol Hydrochloride
Non Proprietary Name: Propranolol
Active Ingredient(s): 60    mg/1 & nbsp;   Propranolol
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Propranolol Hydrochloride

Product NDC: 54868-1517
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078065
Marketing Category: ANDA
Start Marketing Date: 20070330

Package Information of Propranolol Hydrochloride

Package NDC: 54868-1517-2
Package Description: 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-1517-2)

NDC Information of Propranolol Hydrochloride

NDC Code 54868-1517-2
Proprietary Name Propranolol Hydrochloride
Package Description 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-1517-2)
Product NDC 54868-1517
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Propranolol
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20070330
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name PROPRANOLOL HYDROCHLORIDE
Strength Number 60
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Propranolol Hydrochloride


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