What is NDC 59726-125?

59726-125 is the product NDC for Minoxidil, Minoxidil 50 mg/mL aerosol, foam, listed with the FDA by P & L Development, LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.

P & L Development, LLC, NDC labeler code 59726. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Minoxidil?

44 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Minoxidil NDC 59726-125 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)59726-125Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59726-0125Add 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
59726-125-60	5972601256059726012560	1 CAN in 1 PACKAGE (59726-125-60) / 60 mL in 1 CANMarketed from Oct 1, 2023
59726-125-70	5972601257059726012570	3 CAN in 1 PACKAGE (59726-125-70) / 60 mL in 1 CANMarketed from Oct 1, 2023

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/mL
Dosage form: Aerosol, Foam
Route: Topical
Labeler: P & L Development, LLCNDC labeler code 59726
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 208092
Marketing start: Oct 1, 2023
Listing expires: Dec 31, 2027
Other FDA classes: Arteriolar Vasodilation (Physiologic effect)
Identifiers: Product ID 59726-125_5eda5f90-d06c-41a2-b97b-c8e132cc9516SPL ID 5eda5f90-d06c-41a2-b97b-c8e132cc9516SPL set ID 869ce741-3094-4123-9059-0669f3591b2fRxCUI 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

N459726012560 followed by a unit qualifier and the quantity

Package 59726-0125-60. 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 Aug 6, 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)

About NDC 59726-125

What is NDC 59726-125?: 59726-125 is the product NDC for Minoxidil, Minoxidil 50 mg/mL aerosol, foam, listed with the FDA by P & L Development, LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Minoxidil.
What is the active ingredient?: Minoxidil.
Who is the labeler?: P & L Development, LLC, NDC labeler code 59726. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Minoxidil?: 44 other product NDCs are listed under this name. See all Minoxidil NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Minoxidil NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Minoxidilminoxidil foam 5% (womens)	Minoxidil 50 mg/g	Aerosol, FoamTopical	Clarity Cosmetics Inc.	84382-001	84382-0001-04
Minoxidil	Minoxidil 50 mg/g	Aerosol, FoamTopical	P & L Development, LLC	59726-151	59726-0151-6059726-0151-70
Minoxidil	Minoxidil 50 mg/g	Aerosol, FoamTopical	P & L Development, LLC	59726-122	59726-0122-60
Minoxidil	Minoxidil 50 mg/g	Aerosol, FoamTopical	Keranique	70550-116	70550-0116-0270550-0116-20
minoxidil	Minoxidil 50 mg/g	Aerosol, FoamTopical	L. Perrigo Company	0113-5129	00113-5129-0100113-5129-06
Minoxidil	Minoxidil 50 mg/g	Aerosol, FoamTopical	P & L Development, LLC	59726-115	59726-0115-6059726-0115-6559726-0115-70
Minoxidil	Minoxidil 50 mg/g	Aerosol, FoamTopical	P & L Development, LLC	59726-116	59726-0116-6059726-0116-65
Minoxidil	Minoxidil 2 g/100mL	SolutionTopical	Walgreens	0363-9970	00363-9970-0200363-9970-06
Minoxidil	Minoxidil 50 mg/mL	SolutionTopical	Walgreens	0363-9973	00363-9973-06
Minoxidil	Minoxidil 2.5 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8273	68788-8273-03

All 45 Minoxidil NDCs

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	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/g	Aerosol, FoamTopical	P & L Development, LLC	59726-151
Minoxidil	Minoxidil 50 mg/g	Aerosol, FoamTopical	Keranique	70550-116
Minoxidil For Menminoxidil	Minoxidil 50 mg/g	Aerosol, FoamTopical	BosleyMD	69113-501
Minoxidil For Womenminoxidil	Minoxidil 50 mg/g	Aerosol, FoamTopical	BosleyMD	69113-502