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Verapamil Hydrochloride - 63629-3052-1 - (Verapamil Hydrochloride)

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Drug Information of Verapamil Hydrochloride

Product NDC: 63629-3052
Proprietary Name: Verapamil Hydrochloride
Non Proprietary Name: Verapamil Hydrochloride
Active Ingredient(s): 240    mg/1 & nbsp;   Verapamil Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Verapamil Hydrochloride

Product NDC: 63629-3052
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073568
Marketing Category: ANDA
Start Marketing Date: 19920801

Package Information of Verapamil Hydrochloride

Package NDC: 63629-3052-1
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-3052-1)

NDC Information of Verapamil Hydrochloride

NDC Code 63629-3052-1
Proprietary Name Verapamil Hydrochloride
Package Description 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-3052-1)
Product NDC 63629-3052
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Verapamil Hydrochloride
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 19920801
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name VERAPAMIL HYDROCHLORIDE
Strength Number 240
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

Complete Information of Verapamil Hydrochloride


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