up and up hair regrowth treatment for women

Product NDC
11673-431
11-digit product format
116730431
Labeler code
11673
Product ID
11673-431_2a3cf23f-f238-4722-8674-ac7e939de9d6
Type
HUMAN OTC DRUG
Nonproprietary name
Minoxidil
Dosage form
AEROSOL, FOAM
Route
TOPICAL
Labeler
Target Corporation
Application
ANDA091344
Marketing category
ANDA
Marketing start
2018-12-30
Marketing end
0000-00-00
Substance
MINOXIDIL
Active strength
50 mg/g
Pharmacologic classes
Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11673-431UP AND UP HAIR REGROWTH TREATMENT FOR WOMEN (MINOXIDIL) AEROSOL, FOAM [TARGET CORPORATION]5Legacy NDC20220601_0d9ab04a-3952-450e-8fd7-17c9e278135d.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
11673-431-01116730431011 CAN in 1 CARTON (11673-431-01) > 60 g in 1 CAN1 can2018-12-300000-00-00NoNoCurrent
11673-431-02116730431022 CAN in 1 CARTON (11673-431-02) > 60 g in 1 CAN2 can2018-12-300000-00-00NoNoCurrent