up and up hair regrowth treatment for women

Product NDC
11673-382
11-digit product format
116730382
Labeler code
11673
Product ID
11673-382_c92305f6-95e0-4762-b695-e1b8401bb1f4
Type
HUMAN OTC DRUG
Nonproprietary name
minoxidil
Dosage form
SOLUTION
Route
TOPICAL
Labeler
Target Corporation
Application
ANDA075357
Marketing category
ANDA
Marketing start
2021-03-25
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 Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11673-382UP AND UP HAIR REGROWTH TREATMENT FOR WOMEN (MINOXIDIL) SOLUTION [TARGET CORPORATION]2Legacy NDC20210923_6a7124d4-4789-47b2-b29d-8af8af90c515.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
11673-382-16116730382161 BOTTLE in 1 CARTON (11673-382-16) > 60 mL in 1 BOTTLE1 bottle2021-03-250000-00-00NoNoCurrent
11673-382-30116730382303 BOTTLE in 1 CARTON (11673-382-30) > 60 mL in 1 BOTTLE3 bottle2021-03-250000-00-00NoNoCurrent