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Verapamil Hydrochloride - 53808-0329-1 - (Verapamil Hydrochloride)

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Drug Information of Verapamil Hydrochloride

Product NDC: 53808-0329
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, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Verapamil Hydrochloride

Product NDC: 53808-0329
Labeler Name: State of Florida DOH Central Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073568
Marketing Category: ANDA
Start Marketing Date: 20090701

Package Information of Verapamil Hydrochloride

Package NDC: 53808-0329-1
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (53808-0329-1)

NDC Information of Verapamil Hydrochloride

NDC Code 53808-0329-1
Proprietary Name Verapamil Hydrochloride
Package Description 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (53808-0329-1)
Product NDC 53808-0329
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 20090701
Marketing Category Name ANDA
Labeler Name State of Florida DOH Central Pharmacy
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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