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Diltiazem Hydrochloride - 54868-4868-0 - (diltiazem)

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Drug Information of Diltiazem Hydrochloride

Product NDC: 54868-4868
Proprietary Name: Diltiazem Hydrochloride
Non Proprietary Name: diltiazem
Active Ingredient(s): 240    mg/1 & nbsp;   diltiazem
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Diltiazem Hydrochloride

Product NDC: 54868-4868
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074984
Marketing Category: ANDA
Start Marketing Date: 20040524

Package Information of Diltiazem Hydrochloride

Package NDC: 54868-4868-0
Package Description: 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (54868-4868-0)

NDC Information of Diltiazem Hydrochloride

NDC Code 54868-4868-0
Proprietary Name Diltiazem Hydrochloride
Package Description 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (54868-4868-0)
Product NDC 54868-4868
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name diltiazem
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20040524
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name DILTIAZEM HYDROCHLORIDE
Strength Number 240
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

Complete Information of Diltiazem Hydrochloride


General Information