NDC codes

FDA NDC Directory
Product NDC (as listed)83148-021Labeler and product segments. Claims need a package NDC.
Product NDC at billing width83148-0021Add 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 NDC11-digit (billing)PackageCopy
83148-021-60831480021601 TUBE in 1 CARTON (83148-021-60) / 60 g in 1 TUBEMarketed from Feb 1, 2025
83148-021-99831480021991 TUBE in 1 CARTON (83148-021-99) / 100 g in 1 TUBEMarketed from May 1, 2025

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 — .5 mg/g
Dosage form
Ointment
Route
Topical
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 209973
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 83148-021_40294484-39af-a667-e063-6394a90ab281SPL ID 40294484-39af-a667-e063-6394a90ab281SPL set ID 2bbb5200-8355-ba86-e063-6394a90a23b6RxCUI 141850UNII 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

N483148002160 followed by a unit qualifier and the quantity

Package 83148-0021-60. 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 .

Indications (excerpt from the label)

INDICATIONS AND USAGE Desoximetasone Ointment USP, 0.05% 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 209973

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

FDA NDC Directory listings under ANDA 209973
ProductStrengthForm · routeLabelerProduct NDC
DesoximetasoneDesoximetasone .5 mg/gOintmentTopicalBryant Ranch Prepack72162-2629

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