Desoximetasone NDC 50090-5571

NDC codes

FDA NDC Directory

Product NDC (as listed)50090-5571Labeler and product segments. Claims need a package NDC.

Product NDC at billing width50090-5571Add 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
50090-5571-0	50090557100	1 TUBE in 1 CARTON (50090-5571-0) / 15 g in 1 TUBEMarketed from Jun 25, 2021

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): Desoximetasone
Generic name (nonproprietary): desoximetasone
Active ingredients: Desoximetasone — 2.5 mg/g
Dosage form: Cream
Route: Topical
Labeler: A-S Medication Solutions
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 073193
Marketing start: Nov 30, 1990
Listing expires: Dec 31, 2026
Other FDA classes: Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers: Product ID 50090-5571_854be77b-2a59-4141-a411-7931a2a63304SPL ID 854be77b-2a59-4141-a411-7931a2a63304SPL set ID 0e72952e-8e9f-467a-8191-2bc157087d60RxCUI 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

N450090557100 followed by a unit qualifier and the quantity

Package 50090-5571-00. 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 Dec 9, 2023.

Indications (excerpt from the label)

INDICATIONS AND USAGE Desoximetasone cream USP, 0.05%, desoximetasone cream USP, 0.25%, and desoximetasone gel USP, 0.05% are 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 073193

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

FDA NDC Directory listings under ANDA 073193
Product	Strength	Form · route	Labeler	Product NDC
Desoximetasone	Desoximetasone 2.5 mg/g	CreamTopical	Sun Pharmaceutical Industries, Inc.	51672-1270