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Verapamil Hydrochloride - 0172-4285-10 - (Verapamil Hydrochloride)

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Drug Information of Verapamil Hydrochloride

Product NDC: 0172-4285
Proprietary Name: Verapamil Hydrochloride
Non Proprietary Name: Verapamil Hydrochloride
Active Ingredient(s): 120    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: 0172-4285
Labeler Name: IVAX Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073568
Marketing Category: ANDA
Start Marketing Date: 19971010

Package Information of Verapamil Hydrochloride

Package NDC: 0172-4285-10
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (0172-4285-10) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0172-4285-00)

NDC Information of Verapamil Hydrochloride

NDC Code 0172-4285-10
Proprietary Name Verapamil Hydrochloride
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (0172-4285-10) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0172-4285-00)
Product NDC 0172-4285
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 19971010
Marketing Category Name ANDA
Labeler Name IVAX Pharmaceuticals, Inc.
Substance Name VERAPAMIL HYDROCHLORIDE
Strength Number 120
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

Complete Information of Verapamil Hydrochloride


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