TIAZAC - 0456-2616-63 - (diltiazem hydrochloride)

Alphabetical Index


Drug Information of TIAZAC

Product NDC: 0456-2616
Proprietary Name: TIAZAC
Non Proprietary Name: diltiazem hydrochloride
Active Ingredient(s): 360    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: 0456-2616
Labeler Name: Forest Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020401
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20101225

Package Information of TIAZAC

Package NDC: 0456-2616-63
Package Description: 10 BLISTER PACK in 1 CARTON (0456-2616-63) > 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (0456-2616-11)

NDC Information of TIAZAC

NDC Code 0456-2616-63
Proprietary Name TIAZAC
Package Description 10 BLISTER PACK in 1 CARTON (0456-2616-63) > 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (0456-2616-11)
Product NDC 0456-2616
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 AUTHORIZED GENERIC
Labeler Name Forest Laboratories, Inc.
Substance Name DILTIAZEM HYDROCHLORIDE
Strength Number 360
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]

Complete Information of TIAZAC


General Information