Home > National Drug Code (NDC) > Diltiazem Hydrochloride

Diltiazem Hydrochloride - 0378-0135-05 - (diltiazem hydrochloride)

Alphabetical Index


Drug Information of Diltiazem Hydrochloride

Product NDC: 0378-0135
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): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Diltiazem Hydrochloride

Product NDC: 0378-0135
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072838
Marketing Category: ANDA
Start Marketing Date: 20121204

Package Information of Diltiazem Hydrochloride

Package NDC: 0378-0135-05
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0135-05)

NDC Information of Diltiazem Hydrochloride

NDC Code 0378-0135-05
Proprietary Name Diltiazem Hydrochloride
Package Description 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0135-05)
Product NDC 0378-0135
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name diltiazem hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20121204
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals 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


General Information