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Propranolol Hydrochloride - 21695-669-30 - (Propranolol Hydrochloride)

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Drug Information of Propranolol Hydrochloride

Product NDC: 21695-669
Proprietary Name: Propranolol Hydrochloride
Non Proprietary Name: Propranolol Hydrochloride
Active Ingredient(s): 40    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: 21695-669
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070177
Marketing Category: ANDA
Start Marketing Date: 19860101

Package Information of Propranolol Hydrochloride

Package NDC: 21695-669-30
Package Description: 30 TABLET in 1 BOTTLE (21695-669-30)

NDC Information of Propranolol Hydrochloride

NDC Code 21695-669-30
Proprietary Name Propranolol Hydrochloride
Package Description 30 TABLET in 1 BOTTLE (21695-669-30)
Product NDC 21695-669
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Propranolol Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19860101
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name PROPRANOLOL HYDROCHLORIDE
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Propranolol Hydrochloride


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