Mometasone Furoate NDC 51672-1315

NDC codes

FDA NDC Directory

Product NDC (as listed)51672-1315Labeler and product segments. Claims need a package NDC.

Product NDC at billing width51672-1315Add 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
51672-1315-1	51672131501	1 TUBE in 1 CARTON (51672-1315-1) / 15 g in 1 TUBEMarketed from Dec 21, 2004
51672-1315-6	51672131506	1 TUBE in 1 CARTON (51672-1315-6) / 45 g in 1 TUBEMarketed from Dec 21, 2004

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): Mometasone Furoate
Generic name (nonproprietary): mometasone furoate
Active ingredients: Mometasone furoate — 1 mg/g
Dosage form: Cream
Route: Topical
Labeler: Sun Pharmaceutical Industries, Inc.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 076679
Marketing start: Dec 21, 2004
Listing expires: Dec 31, 2026
Other FDA classes: Corticosteroid Hormone Receptor Agonists (Mechanism)Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers: Product ID 51672-1315_3961a44e-34f7-d648-e063-6394a90a974eSPL ID 3961a44e-34f7-d648-e063-6394a90a974eSPL set ID ce61920d-65df-4423-925d-091e624ea32eRxCUI 311753UNII 04201GDN4R
Pharmacologic class: Corticosteroid

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

N451672131501 followed by a unit qualifier and the quantity

Package 51672-1315-01. 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 Jul 7, 2025.

Indications (excerpt from the label)

Mometasone Furoate Cream USP, 0.1% is a corticosteroid indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses in patients 2 years of age or older. Mometasone Furoate Cream USP, 0.1% is a corticosteroid indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses in patients ≥2 years of age.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 076679

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

FDA NDC Directory listings under ANDA 076679
Product	Strength	Form · route	Labeler	Product NDC
Mometasone Furoate	Mometasone furoate 1 mg/g	CreamTopical	Bryant Ranch Prepack	63629-8681
Mometasone Furoate	Mometasone furoate 1 mg/g	CreamTopical	Padagis Israel Pharmaceuticals Ltd	45802-257
Mometasone Furoate	Mometasone furoate 1 mg/g	CreamTopical	Bryant Ranch Prepack	63629-8682
Mometasone Furoate	Mometasone furoate 1 mg/g	CreamTopical	Bryant Ranch Prepack	71335-2873
Mometasone Furoate	Mometasone furoate 1 mg/g	CreamTopical	Proficient Rx LP	63187-288
Mometasone Furoate	Mometasone furoate 1 mg/g	CreamTopical	Bryant Ranch Prepack	72162-1404
Mometasone Furoate	Mometasone furoate 1 mg/g	CreamTopical	Preferred Pharmaceuticals Inc.	68788-8548