Dilacor - 52544-733-01 - (diltiazem hydrochloride)

Alphabetical Index


Drug Information of Dilacor

Product NDC: 52544-733
Proprietary Name: Dilacor
Non Proprietary Name: diltiazem hydrochloride
Active Ingredient(s): 180    mg/1 & nbsp;   diltiazem hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Dilacor

Product NDC: 52544-733
Labeler Name: Watson Pharma, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020092
Marketing Category: NDA
Start Marketing Date: 19920529

Package Information of Dilacor

Package NDC: 52544-733-01
Package Description: 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (52544-733-01)

NDC Information of Dilacor

NDC Code 52544-733-01
Proprietary Name Dilacor
Package Description 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (52544-733-01)
Product NDC 52544-733
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name diltiazem hydrochloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 19920529
Marketing Category Name NDA
Labeler Name Watson Pharma, Inc.
Substance Name DILTIAZEM HYDROCHLORIDE
Strength Number 180
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

Complete Information of Dilacor


General Information