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Diltiazem Hydrochloride - 54868-4970-1 - (diltiazem)

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Drug Information of Diltiazem Hydrochloride

Product NDC: 54868-4970
Proprietary Name: Diltiazem Hydrochloride
Non Proprietary Name: diltiazem
Active Ingredient(s): 120    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: 54868-4970
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074984
Marketing Category: ANDA
Start Marketing Date: 20091218

Package Information of Diltiazem Hydrochloride

Package NDC: 54868-4970-1
Package Description: 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (54868-4970-1)

NDC Information of Diltiazem Hydrochloride

NDC Code 54868-4970-1
Proprietary Name Diltiazem Hydrochloride
Package Description 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (54868-4970-1)
Product NDC 54868-4970
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name diltiazem
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20091218
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name DILTIAZEM HYDROCHLORIDE
Strength Number 120
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

Complete Information of Diltiazem Hydrochloride


General Information