Doxazosin

Product NDC

70518-1061

11-digit product format

705181061

Labeler code

70518

Product ID

70518-1061_a71ab7a9-80d3-61a7-e053-2995a90a1fe0

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Doxazosin Mesylate

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA075536

Marketing category

ANDA

Marketing start

2018-03-13

Marketing end

0000-00-00

Substance

DOXAZOSIN MESYLATE

Active strength

1 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record