up and up hair regrowth treatment for women

Product NDC
11673-189
11-digit product format
116730189
Labeler code
11673
Product ID
11673-189_10b49685-fc4d-489d-96ac-86e4baffbb90
Type
HUMAN OTC DRUG
Nonproprietary name
Minoxidil
Dosage form
SOLUTION
Route
TOPICAL
Labeler
Target Corporation
Application
ANDA075357
Marketing category
ANDA
Marketing start
2015-08-31
Marketing end
0000-00-00
Substance
MINOXIDIL
Active strength
2 g/100mL
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11673-189UP AND UP HAIR REGROWTH TREATMENT FOR WOMEN (MINOXIDIL) SOLUTION [TARGET CORPORATION]4Legacy NDC20210424_b40969a3-3090-41ee-9070-fe0bca047c78.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
11673-189-30116730189303 BOTTLE in 1 CARTON (11673-189-30) > 60 mL in 1 BOTTLE (11673-189-16) 3 bottle2015-08-310000-00-00NoNoCurrent