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Propranolol Hydrochloride - 43478-900-88 - (propranolol hydrochloride)

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Drug Information of Propranolol Hydrochloride

Product NDC: 43478-900
Proprietary Name: Propranolol Hydrochloride
Non Proprietary Name: propranolol hydrochloride
Active Ingredient(s): 60    mg/1 & nbsp;   propranolol hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Propranolol Hydrochloride

Product NDC: 43478-900
Labeler Name: Rouses Point Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018553
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 19830419

Package Information of Propranolol Hydrochloride

Package NDC: 43478-900-88
Package Description: 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (43478-900-88)

NDC Information of Propranolol Hydrochloride

NDC Code 43478-900-88
Proprietary Name Propranolol Hydrochloride
Package Description 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (43478-900-88)
Product NDC 43478-900
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name propranolol hydrochloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 19830419
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Rouses Point Pharmaceuticals, LLC
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


General Information