Alclometasone dipropionate NDC 51672-1306

NDC codes

FDA NDC Directory

Product NDC (as listed)51672-1306Labeler and product segments. Claims need a package NDC.

Product NDC at billing width51672-1306Add 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
51672-1306-1	51672130601	1 TUBE in 1 CARTON (51672-1306-1) / 15 g in 1 TUBEMarketed from Sep 15, 2005
51672-1306-3	51672130603	1 TUBE in 1 CARTON (51672-1306-3) / 60 g in 1 TUBEMarketed from Sep 15, 2005
51672-1306-6	51672130606	1 TUBE in 1 CARTON (51672-1306-6) / 45 g in 1 TUBEMarketed from Sep 15, 2005

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): Alclometasone dipropionate
Generic name (nonproprietary): alclometasone dipropionate
Active ingredients: Alclometasone dipropionate — .5 mg/g
Dosage form: Cream
Route: Topical
Labeler: Sun Pharmaceutical Industries, Inc.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 076587
Marketing start: Sep 15, 2005
Listing expires: Dec 31, 2026
Other FDA classes: Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers: Product ID 51672-1306_3b1658d4-835e-5ae1-e063-6394a90aa7b5SPL ID 3b1658d4-835e-5ae1-e063-6394a90aa7b5SPL set ID 3e688309-880a-4890-bf00-90afd19084f6RxCUI 855474UNII S56PQL4N1VUPC 0351672130619
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

N451672130601 followed by a unit qualifier and the quantity

Package 51672-1306-01. 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 29, 2025.

Indications (excerpt from the label)

INDICATIONS AND USAGE Alclometasone Dipropionate Cream USP, 0.05% is a low to medium potency corticosteroid indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses. Alclometasone dipropionate cream may be used in pediatric patients 1 year of age or older, although the safety and efficacy of drug use for longer than 3 weeks have not been established (see PRECAUTIONS: Pediatric Use ). Since the safety and efficacy of alclometasone dipropionate cream have not been established in pediatric patients below 1 year of age, their use in this age-group is not recommended.

Excerpt only. Read the full label for complete information.

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