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Verapamil Hydrochloride - 0172-4286-70 - (Verapamil Hydrochloride)

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Drug Information of Verapamil Hydrochloride

Product NDC: 0172-4286
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: 0172-4286
Labeler Name: IVAX Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074330
Marketing Category: ANDA
Start Marketing Date: 19940314

Package Information of Verapamil Hydrochloride

Package NDC: 0172-4286-70
Package Description: 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0172-4286-70)

NDC Information of Verapamil Hydrochloride

NDC Code 0172-4286-70
Proprietary Name Verapamil Hydrochloride
Package Description 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0172-4286-70)
Product NDC 0172-4286
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 19940314
Marketing Category Name ANDA
Labeler Name IVAX Pharmaceuticals, 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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