What is NDC 65162-890?

65162-890 is the product NDC for Olopatadine Hydrochloride, Olopatadine hydrochloride 665 ug/1 spray, metered, listed with the FDA by Amneal Pharmaceuticals LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

Amneal Pharmaceuticals LLC, NDC labeler code 65162. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Olopatadine Hydrochloride?

63 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Olopatadine Hydrochloride NDC 65162-890

NDC codes

FDA NDC Directory

Product NDC (as listed)65162-890Labeler and product segments. Claims need a package NDC.

Product NDC at billing width65162-0890Add 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
65162-890-23	65162089023	1 BOTTLE, SPRAY in 1 CARTON (65162-890-23) / 665 SPRAY, METERED in 1 BOTTLE, SPRAYMarketed from Feb 3, 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): Olopatadine Hydrochloride
Generic name (nonproprietary): olopatadine hydrochloride
Active ingredients: Olopatadine hydrochloride — 665 ug/1
Dosage form: Spray, Metered
Route: Nasal
Labeler: Amneal Pharmaceuticals LLCNDC labeler code 65162
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 210901
Marketing start: Feb 3, 2020
Listing expires: Dec 31, 2026
Other FDA classes: Decreased Histamine Release (Physiologic effect)Histamine H1 Receptor Antagonists (Mechanism)
Identifiers: Product ID 65162-890_270f118a-97b1-420b-8504-bfc600008903SPL ID 270f118a-97b1-420b-8504-bfc600008903SPL set ID 806e8d0f-ff42-4d6e-b840-49e3bf867cb5RxCUI 1797895UNII 2XG66W44KF
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. Nasal products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N465162089023 followed by a unit qualifier and the quantity

Package 65162-0890-23. 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 30, 2021.

Indications (excerpt from the label)

Olopatadine hydrochloride (HCl) nasal spray is indicated for the relief of the symptoms of seasonal allergic rhinitis in adults and pediatric patients 6 years of age and older. Olopatadine hydrochloride (HCl) nasal spray is an H 1 receptor antagonist indicated for the relief of the symptoms of seasonal allergic rhinitis in adults and pediatric patients 6 years of age and older (1) .

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 65162-890

What is NDC 65162-890?: 65162-890 is the product NDC for Olopatadine Hydrochloride, Olopatadine hydrochloride 665 ug/1 spray, metered, listed with the FDA by Amneal Pharmaceuticals LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Olopatadine Hydrochloride.
What is the active ingredient?: Olopatadine hydrochloride.
Who is the labeler?: Amneal Pharmaceuticals LLC, NDC labeler code 65162. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Olopatadine Hydrochloride?: 63 other product NDCs are listed under this name. See all Olopatadine 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 Olopatadine Hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Olopatadine Hydrochloride	Olopatadine hydrochloride 2 mg/mL	SolutionOphthalmic	YYBA CORP	73581-713	73581-0713-02
Olopatadine Hydrochloride	Olopatadine hydrochloride 2 mg/mL	SolutionOphthalmic	YYBA CORP	73581-712	73581-0712-02
Olopatadine Hydrochlorideolopatadine hydrochloride ophthalmic	Olopatadine hydrochloride 1 mg/mL	SolutionOphthalmic	AmerisourceBergen Drug Corp	46122-823	46122-0823-29
Olopatadine Hydrochloride	Olopatadine hydrochloride 2 mg/mL	SolutionOphthalmic	AmerisourceBergen Drug Corp	46122-824	46122-0824-29
Olopatadine Hydrochloride	Olopatadine hydrochloride 2 mg/mL	SolutionOphthalmic	YYBA Corp	73581-709	73581-0709-02
Olopatadine Hydrochloride	Olopatadine hydrochloride 2 mg/mL	SolutionOphthalmic	WALGREEN COMPANY	0363-0869	00363-0869-0100363-0869-02
Olopatadine Hydrochloride	Olopatadine hydrochloride 2 mg/mL	SolutionOphthalmic	BluePoint Laboratories	68001-674	68001-0674-92
Olopatadine Hydrochloride	Olopatadine hydrochloride 1 mg/mL	Solution/ dropsOphthalmic	Allegiant Health	69168-480	69168-0480-0269168-0480-65
olopatadine hydrochloride	Olopatadine hydrochloride 2 mg/mL	SolutionOphthalmic	Rising Pharma Holdings, Inc.	16571-861	16571-0861-25
olopatadine hydrochloride	Olopatadine hydrochloride 1 mg/mL	SolutionOphthalmic	Rising Pharma Holdings, Inc.	16571-882	16571-0882-05

All 64 Olopatadine Hydrochloride NDCs