What is NDC 51672-2151?

51672-2151 is the product NDC for Minoxidil Topical Solution, 5% (minoxidil solution), Minoxidil 50 mg/mL solution, listed with the FDA by Sun Pharmaceutical Industries, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Minoxidil Topical Solution, 5% (Minoxidil Solution).

Sun Pharmaceutical Industries, Inc., NDC labeler code 51672. 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 Topical Solution, 5%?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Minoxidil Topical Solution, 5% NDC 51672-2151

NDC codes

FDA NDC Directory

Product NDC (as listed)51672-2151Labeler and product segments. Claims need a package NDC.

Product NDC at billing width51672-2151Add 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
51672-2151-4	51672215104	1 BOTTLE in 1 CARTON (51672-2151-4) / 60 mL in 1 BOTTLEMarketed from Aug 1, 2025
51672-2151-9	51672215109	3 BOTTLE in 1 CARTON (51672-2151-9) / 60 mL in 1 BOTTLEMarketed from Aug 1, 2025

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 Topical Solution, 5%
Generic name (nonproprietary): minoxidil solution
Active ingredients: Minoxidil — 50 mg/mL
Dosage form: Solution
Route: Topical
Labeler: Sun Pharmaceutical Industries, Inc.NDC labeler code 51672
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 217998
Marketing start: Aug 1, 2025
Listing expires: Dec 31, 2027
Other FDA classes: Arteriolar Vasodilation (Physiologic effect)
Identifiers: Product ID 51672-2151_4c37963d-9845-23d1-e063-6394a90aba45SPL ID 4c37963d-9845-23d1-e063-6394a90aba45SPL set ID acc5ad74-4558-4be9-aab4-94ad9ddad6b2RxCUI 311724UNII 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

N451672215104 followed by a unit qualifier and the quantity

Package 51672-2151-04. 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 4, 2026.

Indications (excerpt from the label)

Use to regrow hair on the top of the scalp (vertex only, 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)

About NDC 51672-2151

What is NDC 51672-2151?: 51672-2151 is the product NDC for Minoxidil Topical Solution, 5% (minoxidil solution), Minoxidil 50 mg/mL solution, listed with the FDA by Sun Pharmaceutical Industries, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Minoxidil Topical Solution, 5% (Minoxidil Solution).
What is the active ingredient?: Minoxidil.
Who is the labeler?: Sun Pharmaceutical Industries, Inc., NDC labeler code 51672. 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 Topical Solution, 5%?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other NDCs under ANDA 217998

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

FDA NDC Directory listings under ANDA 217998
Product	Strength	Form · route	Labeler	Product NDC
Keeps Minoxidil Topical Solution, 5%minoxidil solution	Minoxidil 50 mg/mL	SolutionTopical	Keeps (30 Madison)	71713-102

Minoxidil Topical Solution, 5% (Minoxidil solution) NDC 51672-2151