Terazosin - 59746-384-09 - (Terazosin Hydrochloride)

Alphabetical Index


Drug Information of Terazosin

Product NDC: 59746-384
Proprietary Name: Terazosin
Non Proprietary Name: Terazosin Hydrochloride
Active Ingredient(s): 2    mg/1 & nbsp;   Terazosin Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Terazosin

Product NDC: 59746-384
Labeler Name: Jubilant Cadista Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075317
Marketing Category: ANDA
Start Marketing Date: 20041220

Package Information of Terazosin

Package NDC: 59746-384-09
Package Description: 500 CAPSULE in 1 BOTTLE (59746-384-09)

NDC Information of Terazosin

NDC Code 59746-384-09
Proprietary Name Terazosin
Package Description 500 CAPSULE in 1 BOTTLE (59746-384-09)
Product NDC 59746-384
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Terazosin Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20041220
Marketing Category Name ANDA
Labeler Name Jubilant Cadista Pharmaceuticals Inc.
Substance Name TERAZOSIN HYDROCHLORIDE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC]

Complete Information of Terazosin


General Information