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Verapamil Hydrochloride - 49349-623-02 - (Verapamil Hydrochloride)

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Drug Information of Verapamil Hydrochloride

Product NDC: 49349-623
Proprietary Name: Verapamil Hydrochloride
Non Proprietary Name: Verapamil Hydrochloride
Active Ingredient(s): 240    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: 49349-623
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073568
Marketing Category: ANDA
Start Marketing Date: 20111207

Package Information of Verapamil Hydrochloride

Package NDC: 49349-623-02
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (49349-623-02)

NDC Information of Verapamil Hydrochloride

NDC Code 49349-623-02
Proprietary Name Verapamil Hydrochloride
Package Description 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (49349-623-02)
Product NDC 49349-623
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Verapamil Hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20111207
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name VERAPAMIL HYDROCHLORIDE
Strength Number 240
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

Complete Information of Verapamil Hydrochloride


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