NDC codes

FDA NDC Directory
Product NDC (as listed)45802-496Labeler and product segments. Claims need a package NDC.
Product NDC at billing width45802-0496Add 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
45802-496-14458020496141 TUBE in 1 CARTON (45802-496-14) / 15 g in 1 TUBEMarketed from May 14, 2015
45802-496-96458020496961 TUBE in 1 CARTON (45802-496-96) / 60 g in 1 TUBEMarketed from Jun 16, 2015

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
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 077770
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 45802-496_3b8c8718-4be4-4a05-9cf0-f2f4430c675eSPL ID 3b8c8718-4be4-4a05-9cf0-f2f4430c675eSPL set ID 4025ed23-a591-4754-8dbb-4da18f49a3e3RxCUI 197575UNII 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

N445802049614 followed by a unit qualifier and the quantity

Package 45802-0496-14. 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, 0.25% 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 077770

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

FDA NDC Directory listings under ANDA 077770
ProductStrengthForm · routeLabelerProduct NDC
desoximetasoneDesoximetasone 2.5 mg/gOintmentTopicalBryant Ranch Prepack72162-1414
desoximetasoneDesoximetasone 2.5 mg/gOintmentTopicalBryant Ranch Prepack63629-8641
desoximetasoneDesoximetasone 2.5 mg/gOintmentTopicalBryant Ranch Prepack63629-8642

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