Minoxidil

Product NDC: 59450-211
11-digit product format: 594500211
Labeler code: 59450
Product ID: 59450-211_41419988-5dbf-4f47-92d0-0f6f6b6513e9
Type: HUMAN OTC DRUG
Nonproprietary name: Minoxidil
Dosage form: AEROSOL, FOAM
Route: TOPICAL
Labeler: Kroger Company
Application: ANDA209074
Marketing category: ANDA
Marketing start: 2022-10-18
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#

Ingredient, Strength table
Ingredient	Strength
MINOXIDIL	50 mg/g

Field, Values table
Field	Values
Unii	5965120SH1
Rxcui	645146

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
59450-211-01	Minoxidil (For Women)	60 g in 1 CAN	AEROSOL, FOAM	60		2
59450-211-02	Minoxidil (For Women)	2 in 1 CARTON	AEROSOL, FOAM	2		2

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
59450-211	MINOXIDIL (FOR WOMEN) (MINOXIDIL) AEROSOL, FOAM [KROGER COMPANY]	2	Current NDC, Legacy NDC, 2 package rows	20221102_c443fadd-669e-4d29-8b11-ef3c022ca6f4.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
5965120SH1	MINOXIDIL	38304-91-5	MINOXIDIL

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
645146	minoxidil 5 % Topical Foam	PSN	c443fadd-669e-4d29-8b11-ef3c022ca6f4	2
645146	minoxidil 50 MG/ML Topical Foam	SCD	c443fadd-669e-4d29-8b11-ef3c022ca6f4	2
645146	minoxidil 5 % Topical Foam	SY	c443fadd-669e-4d29-8b11-ef3c022ca6f4	2

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
59450-211-01	59450021101	60 g in 1 CAN	60 g					Historical
59450-211-02	59450021102	2 CAN in 1 CARTON (59450-211-02) / 60 g in 1 CAN (59450-211-01)	2 can	2022-10-18	0000-00-00	No	No	Current