TIAZAC - 0456-2615-07 - (diltiazem hydrochloride)

Alphabetical Index


Drug Information of TIAZAC

Product NDC: 0456-2615
Proprietary Name: TIAZAC
Non Proprietary Name: diltiazem hydrochloride
Active Ingredient(s): 300    mg/1 & nbsp;   diltiazem hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of TIAZAC

Product NDC: 0456-2615
Labeler Name: Forest Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020401
Marketing Category: NDA
Start Marketing Date: 20101225

Package Information of TIAZAC

Package NDC: 0456-2615-07
Package Description: 7 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (0456-2615-07)

NDC Information of TIAZAC

NDC Code 0456-2615-07
Proprietary Name TIAZAC
Package Description 7 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (0456-2615-07)
Product NDC 0456-2615
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name diltiazem hydrochloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20101225
Marketing Category Name NDA
Labeler Name Forest Laboratories, Inc.
Substance Name DILTIAZEM HYDROCHLORIDE
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

Complete Information of TIAZAC


General Information