Minoxidil

Product NDC

0615-7593

11-digit product format

006157593

Labeler code

0615

Product ID

0615-7593_4fe14aa2-eafb-4a3f-b04c-c0d9cb90b5e4

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Minoxidil

Dosage form

TABLET

Route

ORAL

Labeler

NCS HealthCare of KY, Inc dba Vangard Labs

Application

ANDA071826

Marketing category

ANDA

Marketing start

1988-11-14

Marketing end

0000-00-00

Substance

MINOXIDIL

Active strength

3 mg/1

Pharmacologic classes

Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record