Doxazosin

Product NDC

68788-9675

11-digit product format

687889675

Labeler code

68788

Product ID

68788-9675_c0e08bc8-57e4-4b7f-a080-fec20868e4ef

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Doxazosin

Dosage form

TABLET

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA075580

Marketing category

ANDA

Marketing start

2013-06-24

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

2019-12-31

Current FDA listing

Historical FDA.report record