Amcinonide NDC 51672-4060

NDC codes

FDA NDC Directory

Product NDC (as listed)51672-4060Labeler and product segments. Claims need a package NDC.

Product NDC at billing width51672-4060Add 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
51672-4060-1	51672406001	1 TUBE in 1 CARTON (51672-4060-1) / 15 g in 1 TUBEMarketed from Mar 19, 2003
51672-4060-2	51672406002	1 TUBE in 1 CARTON (51672-4060-2) / 30 g in 1 TUBEMarketed from Mar 19, 2003
51672-4060-3	51672406003	1 TUBE in 1 CARTON (51672-4060-3) / 60 g in 1 TUBEMarketed from Mar 19, 2003

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): Amcinonide
Generic name (nonproprietary): amcinonide
Active ingredients: Amcinonide — 1 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 076367
Marketing start: Mar 19, 2003
Listing expires: Dec 31, 2026
Other FDA classes: Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers: Product ID 51672-4060_31e404cb-aac7-730b-e063-6394a90afc03SPL ID 31e404cb-aac7-730b-e063-6394a90afc03SPL set ID ac5c3e79-52f7-434e-92ae-24bd32b45edcRxCUI 197327, 197328UNII 423W026MA9
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

N451672406001 followed by a unit qualifier and the quantity

Package 51672-4060-01. 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 Apr 3, 2025.

Indications (excerpt from the label)

INDICATIONS AND USAGE Topical corticosteroids are indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses.

Excerpt only. Read the full label for complete information.

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