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Verapamil Hydrochloride - 54868-5984-1 - (verapamil hydrochloride)

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Drug Information of Verapamil Hydrochloride

Product NDC: 54868-5984
Proprietary Name: Verapamil Hydrochloride
Non Proprietary Name: verapamil hydrochloride
Active Ingredient(s): 360    mg/1 & nbsp;   verapamil hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, DELAYED RELEASE PELLETS
Coding System: National Drug Codes(NDC)

Labeler Information of Verapamil Hydrochloride

Product NDC: 54868-5984
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019614
Marketing Category: NDA
Start Marketing Date: 20090212

Package Information of Verapamil Hydrochloride

Package NDC: 54868-5984-1
Package Description: 10 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (54868-5984-1)

NDC Information of Verapamil Hydrochloride

NDC Code 54868-5984-1
Proprietary Name Verapamil Hydrochloride
Package Description 10 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (54868-5984-1)
Product NDC 54868-5984
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name verapamil hydrochloride
Dosage Form Name CAPSULE, DELAYED RELEASE PELLETS
Route Name ORAL
Start Marketing Date 20090212
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name VERAPAMIL HYDROCHLORIDE
Strength Number 360
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

Complete Information of Verapamil Hydrochloride


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