DILTZAC - 60505-0213-9 - (Diltiazem Hydrochloride)

Alphabetical Index


Drug Information of DILTZAC

Product NDC: 60505-0213
Proprietary Name: DILTZAC
Non Proprietary Name: Diltiazem Hydrochloride
Active Ingredient(s): 300    mg/1 & nbsp;   Diltiazem Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of DILTZAC

Product NDC: 60505-0213
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076395
Marketing Category: ANDA
Start Marketing Date: 20090203

Package Information of DILTZAC

Package NDC: 60505-0213-9
Package Description: 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (60505-0213-9)

NDC Information of DILTZAC

NDC Code 60505-0213-9
Proprietary Name DILTZAC
Package Description 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (60505-0213-9)
Product NDC 60505-0213
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diltiazem Hydrochloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20090203
Marketing Category Name ANDA
Labeler Name Apotex Corp.
Substance Name DILTIAZEM HYDROCHLORIDE
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

Complete Information of DILTZAC


General Information