NDC 59726-122 – Minoxidil

Minoxidil 50 mg/g · Aerosol, Foam · Topical

Human Otc Drug

Product NDC59726-122

Product details

Brand name
Minoxidil
Generic name
Minoxidil
Labeler
P & L Development, LLC
Dosage form
Aerosol, Foam
Route
Topical
Marketing category
ANDA · ANDA208092
Marketed since
May 31, 2024
Listing expires
December 31, 2027
Pharmacologic class
Arteriolar Vasodilator

Active ingredients

Uses, dosage, side effects and warnings for Minoxidil →

Package NDC codes (1)

Package NDCDescriptionSince
59726-122-601 CAN in 1 PACKAGE (59726-122-60) / 60 g in 1 CANMay 31, 2024

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