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Verapamil Hydrochloride - 62175-485-37 - (Verapamil Hydrochloride)

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Drug Information of Verapamil Hydrochloride

Product NDC: 62175-485
Proprietary Name: Verapamil Hydrochloride
Non Proprietary Name: Verapamil Hydrochloride
Active Ingredient(s): 100    mg/1 & nbsp;   Verapamil Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, GELATIN COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Verapamil Hydrochloride

Product NDC: 62175-485
Labeler Name: Kremers Urban Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020943
Marketing Category: NDA
Start Marketing Date: 19981125

Package Information of Verapamil Hydrochloride

Package NDC: 62175-485-37
Package Description: 100 CAPSULE, GELATIN COATED in 1 BOTTLE (62175-485-37)

NDC Information of Verapamil Hydrochloride

NDC Code 62175-485-37
Proprietary Name Verapamil Hydrochloride
Package Description 100 CAPSULE, GELATIN COATED in 1 BOTTLE (62175-485-37)
Product NDC 62175-485
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Verapamil Hydrochloride
Dosage Form Name CAPSULE, GELATIN COATED
Route Name ORAL
Start Marketing Date 19981125
Marketing Category Name NDA
Labeler Name Kremers Urban Pharmaceuticals Inc.
Substance Name VERAPAMIL HYDROCHLORIDE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

Complete Information of Verapamil Hydrochloride


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