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Verapamil Hydrochloride - 52125-123-02 - (verapamil hydrochloride)

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Drug Information of Verapamil Hydrochloride

Product NDC: 52125-123
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: 52125-123
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074587
Marketing Category: ANDA
Start Marketing Date: 20130314

Package Information of Verapamil Hydrochloride

Package NDC: 52125-123-02
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (52125-123-02)

NDC Information of Verapamil Hydrochloride

NDC Code 52125-123-02
Proprietary Name Verapamil Hydrochloride
Package Description 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (52125-123-02)
Product NDC 52125-123
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 20130314
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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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