Olopatadine Hydrochloride NDC 73581-709

NDC codes

FDA NDC Directory

Product NDC (as listed)73581-709Labeler and product segments. Claims need a package NDC.

Product NDC at billing width73581-0709Add 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
73581-709-02	73581070902	2 BOTTLE in 1 CARTON (73581-709-02) / 2.5 mL in 1 BOTTLEMarketed from Mar 1, 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): Olopatadine Hydrochloride
Generic name (nonproprietary): olopatadine hydrochloride
Active ingredients: Olopatadine hydrochloride — 2 mg/mL
Dosage form: Solution
Route: Ophthalmic
Labeler: YYBA Corp
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 219557
Marketing start: Mar 1, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Decreased Histamine Release (Physiologic effect)Histamine H1 Receptor Antagonists (Mechanism)
Identifiers: Product ID 73581-709_49eedab1-1b39-61af-e063-6394a90a2dc6SPL ID 49eedab1-1b39-61af-e063-6394a90a2dc6SPL set ID 47f8ae9b-d92b-4bcb-e063-6294a90af45aRxCUI 1111343UNII 2XG66W44KFUPC 0373581000876
Pharmacologic class: Histamine-1 Receptor Antagonist; Histamine-1 Receptor Inhibitor; Mast Cell Stabilizer

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. Ophthalmic products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N473581070902 followed by a unit qualifier and the quantity

Package 73581-0709-02. 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 Feb 3, 2026.

Indications (excerpt from the label)

Use temporarily relieves itchy eyes due to pollen, ragweed, grass, animal hair and dander

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 219557

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

FDA NDC Directory listings under ANDA 219557
Product	Strength	Form · route	Labeler	Product NDC
Olopatadine Hydrochloride	Olopatadine hydrochloride 2 mg/mL	SolutionOphthalmic	AmerisourceBergen Drug Corp	46122-824
Olopatadine Hydrochloride	Olopatadine hydrochloride 2 mg/mL	SolutionOphthalmic	GLENMARK THERAPEUTICS INC., USA	72657-194
Eye Allergy Itch Relief	Olopatadine hydrochloride 2 mg/mL	Solution/ dropsOphthalmic	Allegiant Health	69168-495
Olopatadine Hydrochloride	Olopatadine hydrochloride 2 mg/mL	SolutionOphthalmic	BluePoint Laboratories	68001-674