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Verapamil Hydrochloride - 54868-6124-1 - (verapamil hydrochloride)

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Drug Information of Verapamil Hydrochloride

Product NDC: 54868-6124
Proprietary Name: Verapamil Hydrochloride
Non Proprietary Name: verapamil hydrochloride
Active Ingredient(s): 200    mg/1 & nbsp;   verapamil hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Verapamil Hydrochloride

Product NDC: 54868-6124
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078306
Marketing Category: ANDA
Start Marketing Date: 20100517

Package Information of Verapamil Hydrochloride

Package NDC: 54868-6124-1
Package Description: 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (54868-6124-1)

NDC Information of Verapamil Hydrochloride

NDC Code 54868-6124-1
Proprietary Name Verapamil Hydrochloride
Package Description 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (54868-6124-1)
Product NDC 54868-6124
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name verapamil hydrochloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20100517
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name VERAPAMIL HYDROCHLORIDE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

Complete Information of Verapamil Hydrochloride


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