berkley and jensen minoxidil

Product NDC
68391-294
11-digit product format
683910294
Labeler code
68391
Product ID
68391-294_7945de8e-6c67-4dfb-9711-630a84a04871
Type
HUMAN OTC DRUG
Nonproprietary name
Minoxidil
Dosage form
AEROSOL, FOAM
Route
TOPICAL
Labeler
BJWC
Application
ANDA091344
Marketing category
ANDA
Marketing start
2018-11-01
Substance
MINOXIDIL
Active strength
5 g/100g
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
berkley and jensen minoxidil
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MINOXIDIL5 g/100g

Harmonized Identifiers#

Field, Values table
FieldValues
Unii5965120SH1
Rxcui645146

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68391-294-04berkley and jensen minoxidil4 in 1 CARTONAEROSOL, FOAM45
68391-294-04berkley and jensen minoxidil60 g in 1 CANAEROSOL, FOAM605

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68391-294BERKLEY AND JENSEN MINOXIDIL (MINOXIDIL) AEROSOL, FOAM [BJWC]5Current NDC, Legacy NDC, 2 package rows20250430_6cfa4553-1d0a-41eb-9059-83b8fac6ddd0.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
645146minoxidil 5 % Topical FoamPSN6cfa4553-1d0a-41eb-9059-83b8fac6ddd05
645146minoxidil 50 MG/ML Topical FoamSCD6cfa4553-1d0a-41eb-9059-83b8fac6ddd05
645146minoxidil 5 % Topical FoamSY6cfa4553-1d0a-41eb-9059-83b8fac6ddd05

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68391-294-04683910294044 CAN in 1 CARTON (68391-294-04) / 60 g in 1 CAN4 can2018-11-010000-00-00NoNoCurrent