DILT-CD - 60505-0009-4 - (diltiazem hydrochloride)

Alphabetical Index


Drug Information of DILT-CD

Product NDC: 60505-0009
Proprietary Name: DILT-CD
Non Proprietary Name: diltiazem hydrochloride
Active Ingredient(s): 240    mg/1 & nbsp;   diltiazem hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of DILT-CD

Product NDC: 60505-0009
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076151
Marketing Category: ANDA
Start Marketing Date: 20060830

Package Information of DILT-CD

Package NDC: 60505-0009-4
Package Description: 90 CAPSULE in 1 BOTTLE (60505-0009-4)

NDC Information of DILT-CD

NDC Code 60505-0009-4
Proprietary Name DILT-CD
Package Description 90 CAPSULE in 1 BOTTLE (60505-0009-4)
Product NDC 60505-0009
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name diltiazem hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20060830
Marketing Category Name ANDA
Labeler Name Apotex Corp.
Substance Name DILTIAZEM HYDROCHLORIDE
Strength Number 240
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

Complete Information of DILT-CD


General Information