Doxazosin

Product NDC

68071-1889

11-digit product format

680711889

Labeler code

68071

Product ID

68071-1889_4fbed5ca-14c5-61f7-e054-00144ff8d46c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Doxazosin

Dosage form

TABLET

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

ANDA202824

Marketing category

ANDA

Marketing start

2015-04-22

Marketing end

0000-00-00

Substance

DOXAZOSIN MESYLATE

Active strength

2 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