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Propranolol Hydrochloride - 24236-699-20 - (Propranolol Hydrochloride)

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Drug Information of Propranolol Hydrochloride

Product NDC: 24236-699
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: 24236-699
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070176
Marketing Category: ANDA
Start Marketing Date: 20130320

Package Information of Propranolol Hydrochloride

Package NDC: 24236-699-20
Package Description: 100 TABLET in 1 CANISTER (24236-699-20)

NDC Information of Propranolol Hydrochloride

NDC Code 24236-699-20
Proprietary Name Propranolol Hydrochloride
Package Description 100 TABLET in 1 CANISTER (24236-699-20)
Product NDC 24236-699
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Propranolol Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130320
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
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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