Terazosin Hydrochloride Anhydrous

Product NDC

51079-936

11-digit product format

510790936

Labeler code

51079

Product ID

51079-936_9af1cfd2-0dea-a218-e053-2995a90a4efd

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

terazosin hydrochloride anhydrous

Dosage form

CAPSULE

Route

ORAL

Labeler

Mylan Institutional Inc.

Application

ANDA075140

Marketing category

ANDA

Marketing start

2000-04-01

Marketing end

2021-01-31

Substance

TERAZOSIN HYDROCHLORIDE ANHYDROUS

Active strength

1 mg/1

Pharmacologic classes

Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record