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Diltiazem Hydrochloride - 0615-3550-39 - (Diltiazem Hydrochloride)

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Drug Information of Diltiazem Hydrochloride

Product NDC: 0615-3550
Proprietary Name: Diltiazem Hydrochloride
Non Proprietary Name: Diltiazem Hydrochloride
Active Ingredient(s): 90    mg/1 & nbsp;   Diltiazem Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Diltiazem Hydrochloride

Product NDC: 0615-3550
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072838
Marketing Category: ANDA
Start Marketing Date: 20121204

Package Information of Diltiazem Hydrochloride

Package NDC: 0615-3550-39
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-3550-39)

NDC Information of Diltiazem Hydrochloride

NDC Code 0615-3550-39
Proprietary Name Diltiazem Hydrochloride
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-3550-39)
Product NDC 0615-3550
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diltiazem Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20121204
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name DILTIAZEM HYDROCHLORIDE
Strength Number 90
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

Complete Information of Diltiazem Hydrochloride


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