Minoxidil for Women

Product NDC

59779-066

11-digit product format

597790066

Labeler code

59779

Product ID

59779-066_5c0f39fa-1789-4599-8089-b95417c25e23

Type

HUMAN OTC DRUG

Nonproprietary name

Minoxidil

Dosage form

SOLUTION

Route

TOPICAL

Labeler

CVS Pharmacy

Application

ANDA074588

Marketing category

ANDA

Marketing start

2003-01-01

Marketing end

2019-06-30

Substance

MINOXIDIL

Active strength

2 g/100mL

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record