Prazosin

Product NDC

50090-3072

11-digit product format

500903072

Labeler code

50090

Product ID

50090-3072_03f98746-5fe7-49d0-a760-abcb9e17083d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

prazosin hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

A-S Medication Solutions

Application

NDA017442

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2017-01-16

Marketing end

0000-00-00

Substance

PRAZOSIN HYDROCHLORIDE

Active strength

2 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record