Desoximetasone NDC 63187-646

NDC codes

FDA NDC Directory

Product NDC (as listed)63187-646Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63187-0646Add 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
63187-646-15	63187064615	1 TUBE in 1 CARTON (63187-646-15) / 15 g in 1 TUBEMarketed from Dec 1, 2018
63187-646-60	63187064660	1 TUBE in 1 CARTON (63187-646-60) / 60 g in 1 TUBEMarketed from Dec 1, 2018

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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): Desoximetasone
Generic name (nonproprietary): desoximetasone
Active ingredients: Desoximetasone — 2.5 mg/g
Dosage form: Cream
Route: Topical
Labeler: Proficient Rx LP
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 076510
Marketing start: Oct 24, 2006
Listing expires: Dec 31, 2026
Other FDA classes: Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers: Product ID 63187-646_4c6cb7aa-0384-4ff9-b9c8-60d24754d7afSPL ID 4c6cb7aa-0384-4ff9-b9c8-60d24754d7afSPL set ID 4f90b0cd-9443-4940-8781-1a05e42ccbb8RxCUI 197574UNII 4E07GXB7AU
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

N463187064615 followed by a unit qualifier and the quantity

Package 63187-0646-15. 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 Jun 1, 2020.

Indications (excerpt from the label)

INDICATIONS AND USAGE Desoximetasone Cream USP, 0.25% is indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 076510

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

FDA NDC Directory listings under ANDA 076510
Product	Strength	Form · route	Labeler	Product NDC
Desoximetasone	Desoximetasone 2.5 mg/g	CreamTopical	Padagis Israel Pharmaceuticals Ltd	45802-495
Desoximetasone	Desoximetasone 2.5 mg/g	CreamTopical	A-S Medication Solutions	50090-0597
Desoximetasone	Desoximetasone 2.5 mg/g	CreamTopical	Bryant Ranch Prepack	72162-2330