desoximetasone NDC 72578-095

NDC codes

FDA NDC Directory

Product NDC (as listed)72578-095Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72578-0095Add 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
72578-095-01	72578009501	1 TUBE in 1 CARTON (72578-095-01) / 15 g in 1 TUBEMarketed from Oct 23, 2020
72578-095-02	72578009502	1 TUBE in 1 CARTON (72578-095-02) / 60 g in 1 TUBEMarketed from Oct 23, 2020
72578-095-03	72578009503	1 TUBE in 1 CARTON (72578-095-03) / 100 g in 1 TUBEMarketed from Oct 23, 2020

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: Ointment
Route: Topical
Labeler: Viona Pharmaceuticals Inc
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 205206
Marketing start: Oct 23, 2020
Listing expires: Dec 31, 2026
Other FDA classes: Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers: Product ID 72578-095_a4b291f3-d49c-4ff0-b79d-dba724f45037SPL ID a4b291f3-d49c-4ff0-b79d-dba724f45037SPL set ID f8e213a9-5e80-45e2-834c-7734dd39c1acRxCUI 197575UNII 4E07GXB7AUUPC 0372578095017
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

N472578009501 followed by a unit qualifier and the quantity

Package 72578-0095-01. 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 Oct 4, 2022.

Indications (excerpt from the label)

INDICATIONS AND USAGE Desoximetasone Ointment 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 205206

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

FDA NDC Directory listings under ANDA 205206
Product	Strength	Form · route	Labeler	Product NDC
desoximetasone	Desoximetasone 2.5 mg/g	OintmentTopical	Zydus Lifesciences Limited	70771-1166