Fluocinonide NDC 51672-1264

NDC codes

FDA NDC Directory

Product NDC (as listed)51672-1264Labeler and product segments. Claims need a package NDC.

Product NDC at billing width51672-1264Add 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
51672-1264-1	51672126401	1 TUBE in 1 CARTON (51672-1264-1) / 15 g in 1 TUBEMarketed from Jun 30, 1999
51672-1264-2	51672126402	1 TUBE in 1 CARTON (51672-1264-2) / 30 g in 1 TUBEMarketed from Jun 30, 1999
51672-1264-3	51672126403	1 TUBE in 1 CARTON (51672-1264-3) / 60 g in 1 TUBEMarketed from Jun 30, 1999

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 — .5 mg/g
Dosage form: Ointment
Route: Topical
Labeler: Sun Pharmaceutical Industries, Inc.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 075008
Marketing start: Jun 30, 1999
Listing expires: Dec 31, 2026
Other FDA classes: Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers: Product ID 51672-1264_46a43966-e83f-a3cc-e063-6394a90af22dSPL ID 46a43966-e83f-a3cc-e063-6394a90af22dSPL set ID b0bc89a9-c9d5-4adb-9785-2d4487c4c656RxCUI 103456, 103457, 310362, 1801283UNII 2W4A77YPANUPC 0351672126414, 0351672127923
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

N451672126401 followed by a unit qualifier and the quantity

Package 51672-1264-01. 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 Dec 23, 2025.

Indications (excerpt from the label)

INDICATIONS AND USAGE Fluocinonide Cream USP, 0.05%, Fluocinonide Cream USP, 0.05% (Emulsified Base), Fluocinonide Gel USP, 0.05% and Fluocinonide Ointment USP, 0.05% are 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 075008

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

FDA NDC Directory listings under ANDA 075008
Product	Strength	Form · route	Labeler	Product NDC
Fluocinonide	Fluocinonide .5 mg/g	OintmentTopical	Preferred Pharmaceuticals Inc.	68788-8554