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VERAPAMIL HYDROCHLORIDE - 57664-117-88 - (VERAPAMIL HYDROCHLORIDE)

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Drug Information of VERAPAMIL HYDROCHLORIDE

Product NDC: 57664-117
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, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of VERAPAMIL HYDROCHLORIDE

Product NDC: 57664-117
Labeler Name: Caraco Pharmaceutical Laboratories, Ltd.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090529
Marketing Category: ANDA
Start Marketing Date: 20120101

Package Information of VERAPAMIL HYDROCHLORIDE

Package NDC: 57664-117-88
Package Description: 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (57664-117-88)

NDC Information of VERAPAMIL HYDROCHLORIDE

NDC Code 57664-117-88
Proprietary Name VERAPAMIL HYDROCHLORIDE
Package Description 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (57664-117-88)
Product NDC 57664-117
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name VERAPAMIL HYDROCHLORIDE
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20120101
Marketing Category Name ANDA
Labeler Name Caraco Pharmaceutical Laboratories, Ltd.
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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