NDC codes

FDA NDC Directory
Product NDC (as listed)46708-485Labeler and product segments. Claims need a package NDC.
Product NDC at billing width46708-0485Add 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
46708-485-15467080485151 TUBE in 1 CARTON (46708-485-15) / 15 g in 1 TUBEMarketed from Mar 7, 2025
46708-485-60467080485601 TUBE in 1 CARTON (46708-485-60) / 60 g in 1 TUBEMarketed from Mar 7, 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)
Desonide
Generic name (nonproprietary)
desonide
Active ingredients
Desonide — .5 mg/g
Dosage form
Ointment
Route
Topical
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 212473
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 46708-485_98a69c58-33de-41e1-a26f-7a4152605f05SPL ID 98a69c58-33de-41e1-a26f-7a4152605f05SPL set ID 591762b3-f223-49a1-8e65-63e9086110dfRxCUI 204135UNII J280872D1OUPC 0346708485153
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

N446708048515 followed by a unit qualifier and the quantity

Package 46708-0485-15. 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 .

Indications (excerpt from the label)

INDICATIONS AND USAGE Desonide ointment, 0.05% is a low potency corticosteroid indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid responsive dermatoses. It should not be used for longer than two weeks unless directed by a physician.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 212473

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

FDA NDC Directory listings under ANDA 212473
ProductStrengthForm · routeLabelerProduct NDC
DesonideDesonide .5 mg/gOintmentTopicalAlembic Pharmaceuticals Inc.62332-485

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