Prazosin Hydrochloride

Product NDC

55700-492

11-digit product format

557000492

Labeler code

55700

Product ID

55700-492_c167279b-445d-4d70-b5ac-795c3f521e88

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Prazosin Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

ANDA071745

Marketing category

ANDA

Marketing start

2017-01-27

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