Minoxidil For Women (minoxidil) NDC 70000-0753

NDC codes

FDA NDC Directory

Product NDC (as listed)70000-0753Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70000-0753Add 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
70000-0753-1	70000075301	1 CAN in 1 CARTON (70000-0753-1) / 60 g in 1 CANMarketed from Mar 16, 2026

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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 For Women
Generic name (nonproprietary): minoxidil
Active ingredients: Minoxidil — 50 mg/g
Dosage form: Aerosol, Foam
Route: Topical
Labeler: CARDINAL HEALTH 110, LLC. DBA LEADER
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 218616
Marketing start: Mar 16, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Arteriolar Vasodilation (Physiologic effect)
Identifiers: Product ID 70000-0753_33f9e0de-dff1-4a14-8aec-8c842bf34c31SPL ID 33f9e0de-dff1-4a14-8aec-8c842bf34c31SPL set ID 33f9e0de-dff1-4a14-8aec-8c842bf34c31RxCUI 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

N470000075301 followed by a unit qualifier and the quantity

Package 70000-0753-01. 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 Apr 13, 2026.

Indications (excerpt from the label)

Use to regrow hair on the top of the scalp (see pictures on side of this carton)

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

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 5% (For Men)minoxidil	Minoxidil 50 mg/g	Aerosol, FoamTopical	Better Living Brands, LLC	21130-208
Minoxidil For Menminoxidil	Minoxidil 50 mg/g	Aerosol, FoamTopical	CARDINAL HEALTH 110, LLC. DBA LEADER	70000-0754