What is NDC 51672-1262?

51672-1262 is the product NDC for Desoximetasone, Desoximetasone 2.5 mg/g ointment, listed with the FDA by Sun Pharmaceutical Industries, Inc.. It has 4 package NDCs, shown above in 10- and 11-digit form.

Sun Pharmaceutical Industries, Inc., NDC labeler code 51672. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Desoximetasone?

33 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Desoximetasone NDC 51672-1262 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)51672-1262Labeler and product segments. Claims need a package NDC.

Product NDC at billing width51672-1262Add 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
51672-1262-1	5167212620151672126201	1 TUBE in 1 CARTON (51672-1262-1) / 15 g in 1 TUBEMarketed from Jun 7, 1996
51672-1262-2	5167212620251672126202	1 TUBE in 1 CARTON (51672-1262-2) / 30 g in 1 TUBEMarketed from Jun 7, 1996
51672-1262-3	5167212620351672126203	1 TUBE in 1 CARTON (51672-1262-3) / 60 g in 1 TUBEMarketed from Jun 7, 1996
51672-1262-7	5167212620751672126207	1 TUBE in 1 CARTON (51672-1262-7) / 100 g in 1 TUBEMarketed from Jun 7, 1996

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): Desoximetasone
Generic name (nonproprietary): desoximetasone
Active ingredients: Desoximetasone — 2.5 mg/g
Dosage form: Ointment
Route: Topical
Labeler: Sun Pharmaceutical Industries, Inc.NDC labeler code 51672
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 074286
Marketing start: Jun 7, 1996
Listing expires: Dec 31, 2026
Other FDA classes: Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers: Product ID 51672-1262_390832c6-f29f-e683-e063-6394a90a2484SPL ID 390832c6-f29f-e683-e063-6394a90a2484SPL set ID 627031fc-9b91-4854-b08f-f9fc0c73f1deRxCUI 197575UNII 4E07GXB7AU
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

N451672126201 followed by a unit qualifier and the quantity

Package 51672-1262-01. 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 3, 2025.

Indications (excerpt from the label)

INDICATIONS AND USAGE Desoximetasone ointment USP, 0.25% is 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)

About NDC 51672-1262

What is NDC 51672-1262?: 51672-1262 is the product NDC for Desoximetasone, Desoximetasone 2.5 mg/g ointment, listed with the FDA by Sun Pharmaceutical Industries, Inc.. It has 4 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Desoximetasone.
What is the active ingredient?: Desoximetasone.
Who is the labeler?: Sun Pharmaceutical Industries, Inc., NDC labeler code 51672. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Desoximetasone?: 33 other product NDCs are listed under this name. See all Desoximetasone NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Desoximetasone NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Desoximetasone	Desoximetasone 2.5 mg/g	CreamTopical	Saptalis Pharmaceuticals, LLC.	71656-087	71656-0087-1571656-0087-60
Desoximetasone	Desoximetasone .5 mg/g	CreamTopical	Saptalis Pharmaceuticals, LLC.	71656-086	71656-0086-1571656-0086-60
Desoximetasone	Desoximetasone .5 mg/g	OintmentTopical	Bryant Ranch Prepack	72162-2629	72162-2629-0172162-2629-06
Desoximetasone	Desoximetasone .5 mg/g	OintmentTopical	The J. Molner Company LLC	83148-021	83148-0021-6083148-0021-99
desoximetasone	Desoximetasone 2.5 mg/g	OintmentTopical	Viona Pharmaceuticals Inc	72578-095	72578-0095-0172578-0095-0272578-0095-03
desoximetasone	Desoximetasone 2.5 mg/g	CreamTopical	Viona Pharmaceuticals Inc	72578-091	72578-0091-0172578-0091-0272578-0091-03
desoximetasone	Desoximetasone 2.5 mg/g	CreamTopical	Zydus Lifesciences Limited	70771-1437	70771-1437-0070771-1437-0170771-1437-03
desoximetasone	Desoximetasone 2.5 mg/mL	SprayTopical	Bryant Ranch Prepack	63629-8702	63629-8702-01
desoximetasone	Desoximetasone 2.5 mg/mL	SprayTopical	Bryant Ranch Prepack	72162-1427	72162-1427-01
desoximetasone	Desoximetasone 2.5 mg/mL	SprayTopical	Padagis Israel Pharmaceuticals Ltd	45802-807	45802-0807-98

All 34 Desoximetasone NDCs