Doxazosin

Product NDC

70518-1645

11-digit product format

705181645

Labeler code

70518

Product ID

70518-1645_9618c275-df3e-4a99-e053-2a95a90a5b4d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Doxazosin Mesylate

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA075536

Marketing category

ANDA

Marketing start

2018-11-07

Marketing end

0000-00-00

Substance

DOXAZOSIN MESYLATE

Active strength

4 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