What is NDC 68071-5324?

68071-5324 is the product NDC for Minoxidil, Minoxidil 2.5 mg/1 tablet, listed with the FDA by NuCare Pharmaceuticals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

NuCare Pharmaceuticals, Inc., NDC labeler code 68071. 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 68071-5324 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)68071-5324Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68071-5324Add 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
68071-5324-3	6807153240368071532403	30 TABLET in 1 BOTTLE, PLASTIC (68071-5324-3)Marketed from Sep 18, 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
Generic name (nonproprietary): minoxidil
Active ingredients: Minoxidil — 2.5 mg/1
Dosage form: Tablet
Route: Oral
Labeler: NuCare Pharmaceuticals, Inc.NDC labeler code 68071
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 071344
Marketing start: Oct 26, 2009
Listing expires: Dec 31, 2027
Other FDA classes: Arteriolar Vasodilation (Physiologic effect)
Identifiers: Product ID 68071-5324_5bc9f22c-ecc7-176b-e063-6394a90a7685SPL ID 5bc9f22c-ecc7-176b-e063-6394a90a7685
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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N468071532403 followed by a unit qualifier and the quantity

Package 68071-5324-03. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 68071-5324

What is NDC 68071-5324?: 68071-5324 is the product NDC for Minoxidil, Minoxidil 2.5 mg/1 tablet, listed with the FDA by NuCare Pharmaceuticals, Inc.. It has 1 package NDC, 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?: NuCare Pharmaceuticals, Inc., NDC labeler code 68071. 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/mL	Aerosol, FoamTopical	P & L Development, LLC	59726-125	59726-0125-6059726-0125-70
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

All 45 Minoxidil NDCs

Other NDCs under ANDA 071344

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

FDA NDC Directory listings under ANDA 071344
Product	Strength	Form · route	Labeler	Product NDC
Minoxidil	Minoxidil 2.5 mg/1	TabletOral	Proficient Rx LP	71205-757
Minoxidil	Minoxidil 2.5 mg/1	TabletOral	Bryant Ranch Prepack	71335-3174