Minoxidil

Product NDC
82376-6007
11-digit product format
823766007
Labeler code
82376
Product ID
82376-6007_78f0bcf6-b1b3-4f5b-a608-8f1fb0cfd2ca
Type
HUMAN OTC DRUG
Nonproprietary name
Minoxidil
Dosage form
AEROSOL, FOAM
Route
TOPICAL
Labeler
SPAZI INC.
Application
ANDA209074
Marketing category
ANDA
Marketing start
2022-08-30
Substance
MINOXIDIL
Active strength
50 mg/g
Pharmacologic classes
Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Minoxidil
Brand name suffix
(For Women)
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MINOXIDIL50 mg/g

Harmonized Identifiers#

Field, Values table
FieldValues
Unii5965120SH1
Rxcui645146

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82376-6007-2Minoxidil(For Women)2 in 1 CARTONAEROSOL, FOAM24
82376-6007-8Minoxidil(For Women)60 g in 1 CANAEROSOL, FOAM604

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82376-6007MINOXIDIL (FOR WOMEN) (MINOXIDIL) AEROSOL, FOAM [SPAZI INC.]4Current NDC, Legacy NDC, 2 package rows20240124_facdb1c2-c36e-4bcc-a821-f8bad8bb17aa.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
645146minoxidil 5 % Topical FoamPSNfacdb1c2-c36e-4bcc-a821-f8bad8bb17aa4
645146minoxidil 50 MG/ML Topical FoamSCDfacdb1c2-c36e-4bcc-a821-f8bad8bb17aa4
645146minoxidil 5 % Topical FoamSYfacdb1c2-c36e-4bcc-a821-f8bad8bb17aa4

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
82376-6007-2823766007022 CAN in 1 CARTON (82376-6007-2) / 60 g in 1 CAN (82376-6007-8) 2 can2022-08-300000-00-00NoNoCurrent
82376-6007-88237660070860 g in 1 CAN60 gHistorical