Minoxidil 5% (For Men) (minoxidil) NDC 21130-208

NDC codes

FDA NDC Directory

Product NDC (as listed)21130-208Labeler and product segments. Claims need a package NDC.

Product NDC at billing width21130-0208Add 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
21130-208-03	21130020803	3 CAN in 1 CARTON (21130-208-03) / 60 g in 1 CANMarketed from Jul 3, 2026

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 5% (For Men)
Generic name (nonproprietary): minoxidil
Active ingredients: Minoxidil — 50 mg/g
Dosage form: Aerosol, Foam
Route: Topical
Labeler: Better Living Brands, LLC
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 218616
Marketing start: Jul 3, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Arteriolar Vasodilation (Physiologic effect)
Identifiers: Product ID 21130-208_1bea79e7-410c-4ff5-980c-f7d8ce0cceb6SPL ID 1bea79e7-410c-4ff5-980c-f7d8ce0cceb6SPL set ID 53e33414-2aa4-3dbd-e063-6294a90a06b5RxCUI 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

N421130020803 followed by a unit qualifier and the quantity

Package 21130-0208-03. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 218616

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

FDA NDC Directory listings under ANDA 218616
Product	Strength	Form · route	Labeler	Product NDC
Regoxidine (For Men)minoxidil	Minoxidil 50 mg/g	Aerosol, FoamTopical	INNOVUS PHARMACEUTICALS, INC.	57483-165
Regoxidine (For Women)minoxidil	Minoxidil 50 mg/g	Aerosol, FoamTopical	INNOVUS PHARMACEUTICALS, INC.	57483-175
Minoxidil 5% (For Women)minoxidil	Minoxidil 50 mg/g	Aerosol, FoamTopical	Aurohealth LLC	58602-104
Minoxidil 5% (For Women)minoxidil	Minoxidil 50 mg/g	Aerosol, FoamTopical	Aurohealth LLC	58602-607
Minoxidil 5% (For Men)minoxidil	Minoxidil 50 mg/g	Aerosol, FoamTopical	Aurohealth LLC	58602-608
Minoxidil (For Men)minoxidil	Minoxidil 5 g/100g	LiquidTopical	FlexiGo Inc	85524-2611
Nizoral Hair Regrowth Treatment for Menminoxidil	Minoxidil 50 mg/g	Aerosol, FoamTopical	Kramer Laboratories	55505-237
Minoxidil For Womenminoxidil	Minoxidil 50 mg/g	Aerosol, FoamTopical	CARDINAL HEALTH 110, LLC. DBA LEADER	70000-0753
Minoxidil For Menminoxidil	Minoxidil 50 mg/g	Aerosol, FoamTopical	CARDINAL HEALTH 110, LLC. DBA LEADER	70000-0754