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Verapamil Hydrochloride - 54868-2207-2 - (verapamil hydrochloride)

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Drug Information of Verapamil Hydrochloride

Product NDC: 54868-2207
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: 54868-2207
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074587
Marketing Category: ANDA
Start Marketing Date: 20000509

Package Information of Verapamil Hydrochloride

Package NDC: 54868-2207-2
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-2207-2)

NDC Information of Verapamil Hydrochloride

NDC Code 54868-2207-2
Proprietary Name Verapamil Hydrochloride
Package Description 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-2207-2)
Product NDC 54868-2207
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 20000509
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
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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