minoxidil

Product NDC
0113-5129
11-digit product format
001135129
Labeler code
0113
Product ID
0113-5129_f0c2ab65-44cc-4f8f-80a9-f3b4f507670f
Type
HUMAN OTC DRUG
Nonproprietary name
Minoxidil
Dosage form
AEROSOL, FOAM
Route
TOPICAL
Labeler
L. Perrigo Company
Application
ANDA091344
Marketing category
ANDA
Marketing start
2024-03-08
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
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
0113-5129-01minoxidil60 g in 1 CANAEROSOL, FOAM604
0113-5129-06minoxidil6 in 1 CARTONAEROSOL, FOAM64
0113-5129-06minoxidil60 g in 1 CANAEROSOL, FOAM604

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0113-5129MINOXIDIL AEROSOL, FOAM [L. PERRIGO COMPANY]4Current NDC, 3 package rows20240522_ec91e5f2-f9c4-4a1d-a94c-3b7352339dab.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
645146minoxidil 5 % Topical FoamPSNec91e5f2-f9c4-4a1d-a94c-3b7352339dab4
645146minoxidil 50 MG/ML Topical FoamSCDec91e5f2-f9c4-4a1d-a94c-3b7352339dab4
645146minoxidil 5 % Topical FoamSYec91e5f2-f9c4-4a1d-a94c-3b7352339dab4

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
0113-5129-010011351290160 g in 1 CAN (0113-5129-01) 60 g2024-03-08NoNoCurrent
0113-5129-06001135129066 CAN in 1 CARTON (0113-5129-06) / 60 g in 1 CAN6 can2024-03-08NoNoCurrent