Cardizem - 55154-4250-0 - (diltiazem hydrochloride)

Alphabetical Index


Drug Information of Cardizem

Product NDC: 55154-4250
Proprietary Name: Cardizem
Non Proprietary Name: diltiazem hydrochloride
Active Ingredient(s): 180    mg/1 & nbsp;   diltiazem hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Cardizem

Product NDC: 55154-4250
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020062
Marketing Category: NDA
Start Marketing Date: 20010411

Package Information of Cardizem

Package NDC: 55154-4250-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-4250-0) > 1 CAPSULE in 1 BLISTER PACK

NDC Information of Cardizem

NDC Code 55154-4250-0
Proprietary Name Cardizem
Package Description 10 BLISTER PACK in 1 BAG (55154-4250-0) > 1 CAPSULE in 1 BLISTER PACK
Product NDC 55154-4250
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name diltiazem hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20010411
Marketing Category Name NDA
Labeler Name Cardinal Health
Substance Name DILTIAZEM HYDROCHLORIDE
Strength Number 180
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

Complete Information of Cardizem


General Information