What is NDC 70771-1437?

70771-1437 is the product NDC for desoximetasone, Desoximetasone 2.5 mg/g cream, listed with the FDA by Zydus Lifesciences Limited. It has 3 package NDCs, shown above in 10- and 11-digit form.

Zydus Lifesciences Limited, NDC labeler code 70771. 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 70771-1437 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)70771-1437Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70771-1437Add 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
70771-1437-0	7077114370070771143700	1 TUBE in 1 CARTON (70771-1437-0) / 100 g in 1 TUBEMarketed from Feb 12, 2019
70771-1437-1	7077114370170771143701	1 TUBE in 1 CARTON (70771-1437-1) / 15 g in 1 TUBEMarketed from Feb 12, 2019
70771-1437-3	7077114370370771143703	1 TUBE in 1 CARTON (70771-1437-3) / 60 g in 1 TUBEMarketed from Feb 12, 2019

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: Cream
Route: Topical
Labeler: Zydus Lifesciences LimitedNDC labeler code 70771
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 205620
Marketing start: Feb 12, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers: Product ID 70771-1437_0e9fa124-ac31-45e8-a61b-1301bf32b25aSPL ID 0e9fa124-ac31-45e8-a61b-1301bf32b25aSPL set ID b780701b-5572-48bc-a5f4-00248eaddd3bRxCUI 197574UNII 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

N470771143700 followed by a unit qualifier and the quantity

Package 70771-1437-00. 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 Aug 14, 2024.

Full label on DailyMed (opens in a new tab)

About NDC 70771-1437

What is NDC 70771-1437?: 70771-1437 is the product NDC for desoximetasone, Desoximetasone 2.5 mg/g cream, listed with the FDA by Zydus Lifesciences Limited. It has 3 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?: Zydus Lifesciences Limited, NDC labeler code 70771. 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/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
Desoximetasone	Desoximetasone 2.5 mg/mL	SprayTopical	Lupin Pharmaceuticals, Inc.	68180-944	68180-0944-33

All 34 desoximetasone NDCs

Other NDCs under ANDA 205620

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

FDA NDC Directory listings under ANDA 205620
Product	Strength	Form · route	Labeler	Product NDC
desoximetasone	Desoximetasone 2.5 mg/g	CreamTopical	Viona Pharmaceuticals Inc	72578-091