Up and Up minoxidil

Product NDC

11673-856

11-digit product format

116730856

Labeler code

11673

Product ID

11673-856_6ade6331-f2df-4edc-9e56-f756998cbe9d

Type

HUMAN OTC DRUG

Nonproprietary name

Minoxidil

Dosage form

SOLUTION

Route

TOPICAL

Labeler

Target Corporation

Application

ANDA075357

Marketing category

ANDA

Marketing start

2009-05-27

Marketing end

0000-00-00

Substance

MINOXIDIL

Active strength

2 g/100mL

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record