Cardizem - 0187-0771-55 - (Diltiazem Hydrochloride)

Alphabetical Index


Drug Information of Cardizem

Product NDC: 0187-0771
Proprietary Name: Cardizem
Non Proprietary Name: Diltiazem Hydrochloride
Active Ingredient(s): 30    mg/1 & nbsp;   Diltiazem Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Cardizem

Product NDC: 0187-0771
Labeler Name: Valeant Pharmaceuticals North America LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018602
Marketing Category: NDA
Start Marketing Date: 20101225

Package Information of Cardizem

Package NDC: 0187-0771-55
Package Description: 500 TABLET, COATED in 1 BOTTLE (0187-0771-55)

NDC Information of Cardizem

NDC Code 0187-0771-55
Proprietary Name Cardizem
Package Description 500 TABLET, COATED in 1 BOTTLE (0187-0771-55)
Product NDC 0187-0771
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diltiazem Hydrochloride
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20101225
Marketing Category Name NDA
Labeler Name Valeant Pharmaceuticals North America LLC
Substance Name DILTIAZEM HYDROCHLORIDE
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

Complete Information of Cardizem


General Information