NDC codes

FDA NDC Directory
Product NDC (as listed)63629-8685Labeler and product segments. Claims need a package NDC.
Product NDC at billing width63629-8685Add 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
63629-8685-1636298685011 BOTTLE in 1 CARTON (63629-8685-1) / 30 mL in 1 BOTTLEMarketed from Feb 2, 2009

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)
Mometasone Furoate
Generic name (nonproprietary)
mometasone furoate
Active ingredients
Mometasone furoate — 1 mg/mL
Dosage form
Solution
Route
Topical
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 077180
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 63629-8685_8a2a552e-8cc7-4a5b-9921-ab917a040962SPL ID 8a2a552e-8cc7-4a5b-9921-ab917a040962SPL set ID 5f1f2136-9e10-4d43-bb35-ed285c744fe4RxCUI 151030UNII 04201GDN4R
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

N463629868501 followed by a unit qualifier and the quantity

Package 63629-8685-01. 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)

Mometasone Furoate Topical Solution 0.1% is a corticosteroid indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses in patients 12 years of age or older. Mometasone Furoate Topical Solution 0.1% is a corticosteroid indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses in patients ≥ 12 years of age.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 077180

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

FDA NDC Directory listings under ANDA 077180
ProductStrengthForm · routeLabelerProduct NDC
Mometasone FuroateMometasone furoate 1 mg/mLSolutionTopicalBryant Ranch Prepack72162-1392
Mometasone FuroateMometasone furoate 1 mg/mLSolutionTopicalPadagis Israel Pharmaceuticals Ltd45802-118
Mometasone FuroateMometasone furoate 1 mg/mLSolutionTopicalBryant Ranch Prepack63629-8686

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