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Diltiazem Hydrochloride - 0093-0318-01 - (Diltiazem Hydrochloride)

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Drug Information of Diltiazem Hydrochloride

Product NDC: 0093-0318
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, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Diltiazem Hydrochloride

Product NDC: 0093-0318
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074185
Marketing Category: ANDA
Start Marketing Date: 19951222

Package Information of Diltiazem Hydrochloride

Package NDC: 0093-0318-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (0093-0318-01)

NDC Information of Diltiazem Hydrochloride

NDC Code 0093-0318-01
Proprietary Name Diltiazem Hydrochloride
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (0093-0318-01)
Product NDC 0093-0318
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diltiazem Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19951222
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
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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