NDC codes

FDA NDC Directory
Product NDC (as listed)63629-2337Labeler and product segments. Claims need a package NDC.
Product NDC at billing width63629-2337Add 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
63629-2337-1636292337011 TUBE in 1 CARTON (63629-2337-1) / 60 g in 1 TUBEMarketed from Apr 19, 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)
Fluocinonide
Generic name (nonproprietary)
fluocinonide
Active ingredients
Fluocinonide — .05 mg/g
Dosage form
Ointment
Route
Topical
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 212976
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 63629-2337_813a433f-8108-434b-a275-f59fe7164752SPL ID 813a433f-8108-434b-a275-f59fe7164752SPL set ID 9ee44ed9-e274-4673-8829-0032a36e5b79UNII 2W4A77YPAN
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

N463629233701 followed by a unit qualifier and the quantity

Package 63629-2337-01. 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 .

Indications (excerpt from the label)

INDICATIONS AND USAGE Fluocinonide Ointment 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 212976

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

FDA NDC Directory listings under ANDA 212976
ProductStrengthForm · routeLabelerProduct NDC
FluocinonideFluocinonide .05 mg/gOintmentTopicalXiromed LLC70700-146
FluocinonideFluocinonide .05 mg/gOintmentTopicalBryant Ranch Prepack63629-2338
FluocinonideFluocinonide .05 mg/gOintmentTopicalBryant Ranch Prepack63629-2339
FluocinonideFluocinonide .05 mg/gOintmentTopicalBryant Ranch Prepack72162-1972

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