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Verapamil Hydrochloride - 49349-817-02 - (Verapamil Hydrochloride)

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Drug Information of Verapamil Hydrochloride

Product NDC: 49349-817
Proprietary Name: Verapamil Hydrochloride
Non Proprietary Name: Verapamil Hydrochloride
Active Ingredient(s): 80    mg/1 & nbsp;   Verapamil Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Verapamil Hydrochloride

Product NDC: 49349-817
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070995
Marketing Category: ANDA
Start Marketing Date: 20111116

Package Information of Verapamil Hydrochloride

Package NDC: 49349-817-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-817-02)

NDC Information of Verapamil Hydrochloride

NDC Code 49349-817-02
Proprietary Name Verapamil Hydrochloride
Package Description 30 TABLET in 1 BLISTER PACK (49349-817-02)
Product NDC 49349-817
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Verapamil Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111116
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name VERAPAMIL HYDROCHLORIDE
Strength Number 80
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

Complete Information of Verapamil Hydrochloride


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