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Verapamil Hydrochloride - 0591-2886-01 - (verapamil hydrochloride)

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Drug Information of Verapamil Hydrochloride

Product NDC: 0591-2886
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: 0591-2886
Labeler Name: Watson Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019614
Marketing Category: NDA
Start Marketing Date: 19900529

Package Information of Verapamil Hydrochloride

Package NDC: 0591-2886-01
Package Description: 100 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (0591-2886-01)

NDC Information of Verapamil Hydrochloride

NDC Code 0591-2886-01
Proprietary Name Verapamil Hydrochloride
Package Description 100 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (0591-2886-01)
Product NDC 0591-2886
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name verapamil hydrochloride
Dosage Form Name CAPSULE, DELAYED RELEASE PELLETS
Route Name ORAL
Start Marketing Date 19900529
Marketing Category Name NDA
Labeler Name Watson Laboratories, 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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