Terazosin Hydrochloride

Product NDC

70518-0821

11-digit product format

705180821

Labeler code

70518

Product ID

70518-0821_8edb3ffe-fe41-a3af-e053-2a95a90a4701

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Terazosin Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA074823

Marketing category

ANDA

Marketing start

2017-11-06

Marketing end

0000-00-00

Substance

TERAZOSIN HYDROCHLORIDE

Active strength

5 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record