Fluticasone Propionate NDC 63629-8660

NDC codes

FDA NDC Directory

Product NDC (as listed)63629-8660Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63629-8660Add 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 NDC	11-digit (billing)	Package	Copy
63629-8660-1	63629866001	1 TUBE in 1 CARTON (63629-8660-1) / 60 g in 1 TUBEMarketed from Sep 13, 2006

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): Fluticasone Propionate
Generic name (nonproprietary): fluticasone propionate
Active ingredients: Fluticasone propionate — .5 mg/g
Dosage form: Cream
Route: Topical
Labeler: Bryant Ranch Prepack
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 076793
Marketing start: Sep 13, 2006
Listing expires: Dec 31, 2026
Other FDA classes: Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers: Product ID 63629-8660_00b804f5-76c0-0b1d-e063-6294a90a5753SPL ID 00b804f5-76c0-0b1d-e063-6294a90a5753SPL set ID 8bd6f3a4-87f7-449e-8fcc-fec1537fcab3RxCUI 895987UNII O2GMZ0LF5W
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

N463629866001 followed by a unit qualifier and the quantity

Package 63629-8660-01. 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 Jul 17, 2023.

Indications (excerpt from the label)

INDICATIONS AND USAGE Fluticasone Propionate Cream, 0.05% is a medium potency corticosteroid indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses. Fluticasone Propionate Cream, 0.05% may be used with caution in pediatric patients 3 months of age or older. The safety and efficacy of drug use for longer than 4 weeks in this population have not been established. The safety and efficacy of Fluticasone Propionate Cream, 0.05% in pediatric patients below 3 months of age have not been established.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 076793

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

FDA NDC Directory listings under ANDA 076793
Product	Strength	Form · route	Labeler	Product NDC
Fluticasone Propionate	Fluticasone propionate .5 mg/g	CreamTopical	Bryant Ranch Prepack	72162-1402
Fluticasone Propionate	Fluticasone propionate .5 mg/g	CreamTopical	Bryant Ranch Prepack	63629-8658
Fluticasone Propionate	Fluticasone propionate .5 mg/g	CreamTopical	Bryant Ranch Prepack	63629-8659
Fluticasone Propionate	Fluticasone propionate .5 mg/g	CreamTopical	Padagis Israel Pharmaceuticals Ltd	45802-222
Fluticasone Propionate	Fluticasone propionate .5 mg/g	CreamTopical	A-S Medication Solutions	50090-1187