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Diltiazem Hydrochloride - 63739-079-10 - (Diltiazem Hydrochloride)

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Drug Information of Diltiazem Hydrochloride

Product NDC: 63739-079
Proprietary Name: Diltiazem Hydrochloride
Non Proprietary Name: Diltiazem Hydrochloride
Active Ingredient(s): 30    mg/1 & nbsp;   Diltiazem Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Diltiazem Hydrochloride

Product NDC: 63739-079
Labeler Name: McKesson Packaging Services Business Unit of McKesson Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074185
Marketing Category: ANDA
Start Marketing Date: 20070810

Package Information of Diltiazem Hydrochloride

Package NDC: 63739-079-10
Package Description: 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-079-10) > 10 TABLET, COATED in 1 BLISTER PACK

NDC Information of Diltiazem Hydrochloride

NDC Code 63739-079-10
Proprietary Name Diltiazem Hydrochloride
Package Description 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-079-10) > 10 TABLET, COATED in 1 BLISTER PACK
Product NDC 63739-079
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diltiazem Hydrochloride
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20070810
Marketing Category Name ANDA
Labeler Name McKesson Packaging Services Business Unit of McKesson Corporation
Substance Name DILTIAZEM HYDROCHLORIDE
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

Complete Information of Diltiazem Hydrochloride


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