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Diltiazem Hydrochloride - 51079-925-20 - (diltiazem hydrochloride)

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Drug Information of Diltiazem Hydrochloride

Product NDC: 51079-925
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: 51079-925
Labeler Name: UDL Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074910
Marketing Category: ANDA
Start Marketing Date: 20110816

Package Information of Diltiazem Hydrochloride

Package NDC: 51079-925-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-925-20) > 1 CAPSULE in 1 BLISTER PACK (51079-925-01)

NDC Information of Diltiazem Hydrochloride

NDC Code 51079-925-20
Proprietary Name Diltiazem Hydrochloride
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-925-20) > 1 CAPSULE in 1 BLISTER PACK (51079-925-01)
Product NDC 51079-925
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 UDL Laboratories, Inc.
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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