Cartia - 62037-598-07 - (Diltiazem Hydrochloride)

Alphabetical Index


Drug Information of Cartia

Product NDC: 62037-598
Proprietary Name: Cartia
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 Cartia

Product NDC: 62037-598
Labeler Name: Watson Pharma, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074752
Marketing Category: ANDA
Start Marketing Date: 19990623

Package Information of Cartia

Package NDC: 62037-598-07
Package Description: 7 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62037-598-07)

NDC Information of Cartia

NDC Code 62037-598-07
Proprietary Name Cartia
Package Description 7 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62037-598-07)
Product NDC 62037-598
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Diltiazem Hydrochloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 19990623
Marketing Category Name ANDA
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 Cartia


General Information