What is NDC 58602-522?

58602-522 is the product NDC for Mometasone Furoate, Mometasone furoate monohydrate 50 ug/1 spray, metered, listed with the FDA by Aurohealth LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

What is the active ingredient?

Mometasone furoate monohydrate.

Aurohealth LLC, NDC labeler code 58602. 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?

35 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 58602-522 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)58602-522Labeler and product segments. Claims need a package NDC.

Product NDC at billing width58602-0522Add 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
58602-522-44	5860205224458602052244	1 BOTTLE, SPRAY in 1 CARTON (58602-522-44) / 120 SPRAY, METERED in 1 BOTTLE, SPRAYMarketed from Nov 22, 2024

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 monohydrate — 50 ug/1
Dosage form: Spray, Metered
Route: Nasal
Labeler: Aurohealth LLCNDC labeler code 58602
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 217498
Marketing start: Nov 22, 2024
Listing expires: Dec 31, 2027
Other FDA classes: Corticosteroid Hormone Receptor Agonists (Mechanism)Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers: Product ID 58602-522_48ba8c52-73b6-4ee9-ba13-756a645a9183SPL ID 48ba8c52-73b6-4ee9-ba13-756a645a9183SPL set ID 48ba8c52-73b6-4ee9-ba13-756a645a9183RxCUI 1797865UNII MTW0WEG809UPC 0358602522445
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. Nasal products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N458602052244 followed by a unit qualifier and the quantity

Package 58602-0522-44. 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 Nov 25, 2024.

Indications (excerpt from the label)

Uses temporarily relieves these symptoms of hay fever or other upper respiratory allergies: ■ nasal congestion ■ runny nose ■ sneezing ■ itchy nose

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 58602-522

What is NDC 58602-522?: 58602-522 is the product NDC for Mometasone Furoate, Mometasone furoate monohydrate 50 ug/1 spray, metered, listed with the FDA by Aurohealth LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Mometasone Furoate.
What is the active ingredient?: Mometasone furoate monohydrate.
Who is the labeler?: Aurohealth LLC, NDC labeler code 58602. 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?: 35 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	OintmentTopical	Encube Ethicals, Inc.	21922-071	21922-0071-0421922-0071-06
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 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 Furoatemometasone	Mometasone furoate 50 ug/1	Spray, MeteredNasal	Amneal Pharmaceuticals LLC	65162-891	65162-0891-29
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

All 36 Mometasone Furoate NDCs