What is NDC 51672-2152?

51672-2152 is the product NDC for Minoxidil Topical Solution 2%, Minoxidil 20 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.

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 2%?

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 2% NDC 51672-2152

NDC codes

FDA NDC Directory

Product NDC (as listed)51672-2152Labeler and product segments. Claims need a package NDC.

Product NDC at billing width51672-2152Add 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
51672-2152-4	51672215204	1 BOTTLE in 1 CARTON (51672-2152-4) / 60 mL in 1 BOTTLEMarketed from Sep 1, 2025
51672-2152-9	51672215209	3 BOTTLE in 1 CARTON (51672-2152-9) / 60 mL in 1 BOTTLEMarketed from Sep 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 2%
Generic name (nonproprietary): minoxidil topical solution 2%
Active ingredients: Minoxidil — 20 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 218175
Marketing start: Sep 1, 2025
Listing expires: Dec 31, 2027
Other FDA classes: Arteriolar Vasodilation (Physiologic effect)
Identifiers: Product ID 51672-2152_4c3823f2-ce4b-afea-e063-6294a90a03c0SPL ID 4c3823f2-ce4b-afea-e063-6294a90a03c0SPL set ID 15d7cdd7-6d37-477c-bce7-a459ea960a53RxCUI 311723UNII 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

N451672215204 followed by a unit qualifier and the quantity

Package 51672-2152-04. 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 scalp

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 51672-2152

What is NDC 51672-2152?: 51672-2152 is the product NDC for Minoxidil Topical Solution 2%, Minoxidil 20 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 2%.
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 2%?: 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.