What is NDC 72266-141?

72266-141 is the product NDC for Azelastine Hydrochloride, Azelastine hydrochloride .5 mg/mL solution/ drops, listed with the FDA by Fosun Pharma USA Inc. It has 1 package NDC, shown above in 10- and 11-digit form.

Fosun Pharma USA Inc, NDC labeler code 72266. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Azelastine Hydrochloride?

23 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Azelastine Hydrochloride NDC 72266-141

NDC codes

FDA NDC Directory

Product NDC (as listed)72266-141Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72266-0141Add 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
72266-141-01	7226601410172266014101	1 BOTTLE, PLASTIC in 1 CARTON (72266-141-01) / 6 mL in 1 BOTTLE, PLASTICMarketed from Sep 8, 2020

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): Azelastine Hydrochloride
Generic name (nonproprietary): azelastine hydrochloride
Active ingredients: Azelastine hydrochloride — .5 mg/mL
Dosage form: Solution/ drops
Route: Intraocular
Labeler: Fosun Pharma USA IncNDC labeler code 72266
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 210092
Marketing start: Sep 8, 2020
Listing expires: Dec 31, 2027
Other FDA classes: Histamine H1 Receptor Antagonists (Mechanism)
Identifiers: Product ID 72266-141_4613d423-9c03-f7d0-e063-6394a90a6a9cSPL ID 4613d423-9c03-f7d0-e063-6394a90a6a9cSPL set ID 8ae2aec7-329b-41bf-89d5-f189afb782eeRxCUI 860805UNII 0L591QR10I
Pharmacologic class: Histamine-1 Receptor Antagonist

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N472266014101 followed by a unit qualifier and the quantity

Package 72266-0141-01. 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 Dec 16, 2025.

Indications (excerpt from the label)

INDICATIONS AND USAGE Azelastine hydrochloride ophthalmic solution is indicated for the treatment of itching of the eye associated with allergic conjunctivitis.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72266-141

What is NDC 72266-141?: 72266-141 is the product NDC for Azelastine Hydrochloride, Azelastine hydrochloride .5 mg/mL solution/ drops, listed with the FDA by Fosun Pharma USA Inc. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Azelastine Hydrochloride.
What is the active ingredient?: Azelastine hydrochloride.
Who is the labeler?: Fosun Pharma USA Inc, NDC labeler code 72266. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Azelastine Hydrochloride?: 23 other product NDCs are listed under this name. See all Azelastine Hydrochloride 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 Azelastine Hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Azelastine Hydrochloride	Azelastine hydrochloride 205.5 ug/1	Spray, MeteredNasal	YYBA Corp	73581-500	73581-0500-0173581-0500-02
Azelastine Hydrochloride	Azelastine hydrochloride 137 ug/1	Spray, MeteredNasal	Preferred Pharmaceuticals Inc.	68788-4056	68788-4056-02
Azelastine Hydrochloride	Azelastine hydrochloride 205.5 ug/1	Spray, MeteredNasal	CVS PHARMACY, INC	51316-840	51316-0840-0151316-0840-0251316-0840-03+2 more
Azelastine Hydrochloride	Azelastine hydrochloride 205.5 ug/1	Spray, MeteredNasal	Walgreens	0363-0653	00363-0653-0200363-0653-0300363-0653-04+1 more
Azelastine Hydrochloride	Azelastine hydrochloride 137 ug/1	Spray, MeteredNasal	NorthStar Rx LLC	72603-611	72603-0611-01
Azelastine Hydrochloride	Azelastine hydrochloride 205.5 ug/1	Spray, MeteredNasal	Allegiant Health	69168-478	69168-0478-0269168-0478-63
Azelastine Hydrochloride	Azelastine hydrochloride 205.5 ug/1	Spray, MeteredNasal	Allegiant Health	69168-479	69168-0479-64
Azelastine Hydrochloride	Azelastine hydrochloride 205.5 ug/1	Spray, MeteredNasal	Aurohealth LLC	58602-020	58602-0020-0758602-0020-5158602-0020-52
Azelastine Hydrochloride	Azelastine hydrochloride 137 ug/1	Spray, MeteredNasal	Preferred Pharmaceuticals Inc.	68788-8514	68788-8514-02
Azelastine Hydrochlorideazelastine	Azelastine hydrochloride 1 mg/mL	Spray, MeteredNasal	AvKARE	42291-094	42291-0094-30

All 24 Azelastine Hydrochloride NDCs

Other NDCs under ANDA 210092

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

FDA NDC Directory listings under ANDA 210092
Product	Strength	Form · route	Labeler	Product NDC
Azelastine Hydrochloride	Azelastine hydrochloride .5 mg/mL	Solution/ dropsIntraocular	Gland Pharma Limited	68083-287