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Diltiazem Hydrochloride - 55154-5661-0 - (diltiazem hydrochloride)

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Drug Information of Diltiazem Hydrochloride

Product NDC: 55154-5661
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): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Diltiazem Hydrochloride

Product NDC: 55154-5661
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074910
Marketing Category: ANDA
Start Marketing Date: 20110816

Package Information of Diltiazem Hydrochloride

Package NDC: 55154-5661-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-5661-0) > 1 CAPSULE in 1 BLISTER PACK

NDC Information of Diltiazem Hydrochloride

NDC Code 55154-5661-0
Proprietary Name Diltiazem Hydrochloride
Package Description 10 BLISTER PACK in 1 BAG (55154-5661-0) > 1 CAPSULE in 1 BLISTER PACK
Product NDC 55154-5661
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name diltiazem hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20110816
Marketing Category Name ANDA
Labeler Name Cardinal Health
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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