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Diltiazem Hydrochloride - 76237-148-30 - (diltiazem hydrochloride)

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Drug Information of Diltiazem Hydrochloride

Product NDC: 76237-148
Proprietary Name: Diltiazem Hydrochloride
Non Proprietary Name: diltiazem hydrochloride
Active Ingredient(s): 60    mg/1 & nbsp;   diltiazem hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Diltiazem Hydrochloride

Product NDC: 76237-148
Labeler Name: McKesson Contract Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072838
Marketing Category: ANDA
Start Marketing Date: 20110922

Package Information of Diltiazem Hydrochloride

Package NDC: 76237-148-30
Package Description: 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-148-30) > 5 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Diltiazem Hydrochloride

NDC Code 76237-148-30
Proprietary Name Diltiazem Hydrochloride
Package Description 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-148-30) > 5 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 76237-148
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name diltiazem hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110922
Marketing Category Name ANDA
Labeler Name McKesson Contract Packaging
Substance Name DILTIAZEM HYDROCHLORIDE
Strength Number 60
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

Complete Information of Diltiazem Hydrochloride


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