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Verapamil Hydrochloride - 54868-3300-1 - (verapamil hydrochloride)

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Drug Information of Verapamil Hydrochloride

Product NDC: 54868-3300
Proprietary Name: Verapamil Hydrochloride
Non Proprietary Name: verapamil hydrochloride
Active Ingredient(s): 180    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: 54868-3300
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074587
Marketing Category: ANDA
Start Marketing Date: 19960115

Package Information of Verapamil Hydrochloride

Package NDC: 54868-3300-1
Package Description: 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-3300-1)

NDC Information of Verapamil Hydrochloride

NDC Code 54868-3300-1
Proprietary Name Verapamil Hydrochloride
Package Description 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-3300-1)
Product NDC 54868-3300
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 19960115
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name VERAPAMIL HYDROCHLORIDE
Strength Number 180
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

Complete Information of Verapamil Hydrochloride


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