Minoxidil NDC 59726-151

NDC codes

FDA NDC Directory

Product NDC (as listed)59726-151Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59726-0151Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
59726-151-60	59726015160	1 CAN in 1 PACKAGE (59726-151-60) / 60 g in 1 CANMarketed from Jul 1, 2024
59726-151-70	59726015170	3 CAN in 1 PACKAGE (59726-151-70) / 60 g in 1 CANMarketed from Jul 1, 2024

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Minoxidil
Generic name (nonproprietary): minoxidil
Active ingredients: Minoxidil — 50 mg/g
Dosage form: Aerosol, Foam
Route: Topical
Labeler: P & L Development, LLC
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 208092
Marketing start: Jul 1, 2024
Listing expires: Dec 31, 2027
Other FDA classes: Arteriolar Vasodilation (Physiologic effect)
Identifiers: Product ID 59726-151_a9306a97-00dd-4aba-9f12-5553a7c3e081SPL ID a9306a97-00dd-4aba-9f12-5553a7c3e081SPL set ID 04373c29-85f3-4d7d-bbdd-950dcf1a879aRxCUI 645146UNII 5965120SH1
Pharmacologic class: Arteriolar Vasodilator

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N459726015160 followed by a unit qualifier and the quantity

Package 59726-0151-60. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Mar 3, 2026.

Indications (excerpt from the label)

Use to regrow hair on the top of the scalp (vertex only, see pictures on side of carton)

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 208092

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 208092
Product	Strength	Form · route	Labeler	Product NDC
Minoxidil	Minoxidil 50 mg/g	Aerosol, FoamTopical	Keranique	70550-116
Minoxidil	Minoxidil 50 mg/g	Aerosol, FoamTopical	P & L Development, LLC	59726-115
Minoxidil	Minoxidil 50 mg/g	Aerosol, FoamTopical	P & L Development, LLC	59726-116
Minoxidil	Minoxidil 50 mg/g	Aerosol, FoamTopical	P & L Development, LLC	59726-122
Minoxidil	Minoxidil 50 mg/mL	Aerosol, FoamTopical	P & L Development, LLC	59726-125
Minoxidil For Menminoxidil	Minoxidil 50 mg/g	Aerosol, FoamTopical	BosleyMD	69113-501
Minoxidil For Womenminoxidil	Minoxidil 50 mg/g	Aerosol, FoamTopical	BosleyMD	69113-502