What is NDC 21922-071?

21922-071 is the product NDC for Mometasone furoate, Mometasone furoate 1 mg/g ointment, listed with the FDA by Encube Ethicals, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.

Encube Ethicals, Inc., NDC labeler code 21922. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Mometasone furoate?

34 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Mometasone furoate NDC 21922-071 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)21922-071Labeler and product segments. Claims need a package NDC.

Product NDC at billing width21922-0071Add 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	Copy
21922-071-04	21922007104	1 TUBE in 1 CARTON (21922-071-04) / 15 g in 1 TUBEMarketed from Apr 7, 2026
21922-071-06	21922007106	1 TUBE in 1 CARTON (21922-071-06) / 45 g in 1 TUBEMarketed from Apr 7, 2026

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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): Mometasone furoate
Generic name (nonproprietary): mometasone furoate
Active ingredients: Mometasone furoate — 1 mg/g
Dosage form: Ointment
Route: Topical
Labeler: Encube Ethicals, Inc.NDC labeler code 21922
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 076481
Marketing start: Apr 7, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Corticosteroid Hormone Receptor Agonists (Mechanism)Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers: Product ID 21922-071_2221a9e5-8710-4939-aa22-c9a4033d9f06SPL ID 2221a9e5-8710-4939-aa22-c9a4033d9f06SPL set ID dae3eaea-fc17-48a2-ae30-2a68f7811bceRxCUI 151029UNII 04201GDN4R
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

N421922007104 followed by a unit qualifier and the quantity

Package 21922-0071-04. 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 6, 2026.

Indications (excerpt from the label)

Mometasone furoate ointment USP, 0.1% is a corticosteroid indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses in patients 2 years of age or older. Mometasone furoate ointment USP, 0.1% is a corticosteroid indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses in patients ≥2 years of age.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 21922-071

What is NDC 21922-071?: 21922-071 is the product NDC for Mometasone furoate, Mometasone furoate 1 mg/g ointment, listed with the FDA by Encube Ethicals, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Mometasone furoate.
What is the active ingredient?: Mometasone furoate.
Who is the labeler?: Encube Ethicals, Inc., NDC labeler code 21922. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Mometasone furoate?: 34 other product NDCs are listed under this name. See all Mometasone furoate 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 Mometasone furoate NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Mometasone Furoate	Mometasone furoate 1 mg/g	CreamTopical	Preferred Pharmaceuticals Inc.	68788-4075	68788-4075-04
Mometasone Furoate	Mometasone furoate 1 mg/mL	LotionTopical	Encube Ethicals, Inc.	21922-072	21922-0072-0121922-0072-21
Mometasone Furoate	Mometasone furoate 1 mg/1	OintmentTopical	Torrent Pharmaceuticals Limited	13668-527	13668-0527-0113668-0527-04
Mometasone Furoate	Mometasone furoate monohydrate 50 ug/1	Spray, MeteredNasal	Aurohealth LLC	58602-522	58602-0522-44
Mometasone Furoate	Mometasone furoate 1 mg/g	CreamTopical	Preferred Pharmaceuticals Inc.	68788-8548	68788-8548-04
Mometasone Furoate	Mometasone furoate 1 mg/g	OintmentTopical	Preferred Pharmaceuticals Inc.	68788-8357	68788-8357-04
Mometasone Furoate	Mometasone furoate 1 mg/mL	LotionTopical	Glenmark Pharmaceuticals Inc., USA	68462-385	68462-0385-0268462-0385-37
Mometasone Furoate	Mometasone 50 ug/1	Spray, MeteredNasal	Golden State Medical Supply, Inc.	60429-664	60429-0664-17
Mometasone Furoate	Mometasone 50 ug/1	Spray, MeteredNasal	Apotex Corp.	60505-0830	60505-0830-01
Mometasone Furoate	Mometasone furoate 1 mg/g	OintmentTopical	Cosette Pharmaceuticals, Inc.	0713-0635	00713-0635-1500713-0635-37

All 35 Mometasone furoate NDCs