Prazosin Hydrochloride

Product NDC

50090-3533

11-digit product format

500903533

Labeler code

50090

Product ID

50090-3533_fe7013c6-182a-4cbf-8338-7ff6db2b8c12

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Prazosin Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA071745

Marketing category

ANDA

Marketing start

2007-02-22

Marketing end

0000-00-00

Substance

PRAZOSIN HYDROCHLORIDE

Active strength

1 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