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Diltiazem Hydrochloride - 55154-2051-0 - (Diltiazem Hydrochloride)

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Drug Information of Diltiazem Hydrochloride

Product NDC: 55154-2051
Proprietary Name: Diltiazem Hydrochloride
Non Proprietary Name: Diltiazem Hydrochloride
Active Ingredient(s): 120    mg/1 & nbsp;   Diltiazem Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Diltiazem Hydrochloride

Product NDC: 55154-2051
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074984
Marketing Category: ANDA
Start Marketing Date: 20100115

Package Information of Diltiazem Hydrochloride

Package NDC: 55154-2051-0
Package Description: 1 BLISTER PACK in 1 BAG (55154-2051-0) > 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK

NDC Information of Diltiazem Hydrochloride

NDC Code 55154-2051-0
Proprietary Name Diltiazem Hydrochloride
Package Description 1 BLISTER PACK in 1 BAG (55154-2051-0) > 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC 55154-2051
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diltiazem Hydrochloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20100115
Marketing Category Name ANDA
Labeler Name Cardinal Health
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


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