What is NDC 16571-882?

16571-882 is the product NDC for olopatadine hydrochloride, Olopatadine hydrochloride 1 mg/mL solution, listed with the FDA by Rising Pharma Holdings, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

Rising Pharma Holdings, Inc., NDC labeler code 16571. 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 16571-882

NDC codes

FDA NDC Directory

Product NDC (as listed)16571-882Labeler and product segments. Claims need a package NDC.

Product NDC at billing width16571-0882Add 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
16571-882-05	1657108820516571088205	1 CONTAINER in 1 CARTON (16571-882-05) / 5 mL in 1 CONTAINERMarketed from May 1, 2025

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 — 1 mg/mL
Dosage form: Solution
Route: Ophthalmic
Labeler: Rising Pharma Holdings, Inc.NDC labeler code 16571
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 204392
Marketing start: May 1, 2025
Listing expires: Dec 31, 2026
Other FDA classes: Decreased Histamine Release (Physiologic effect)Histamine H1 Receptor Antagonists (Mechanism)
Identifiers: Product ID 16571-882_c23fbb1d-8ba4-4375-aedf-f2346dde7746SPL ID c23fbb1d-8ba4-4375-aedf-f2346dde7746SPL set ID 7c86e2d4-2d37-4ccf-9227-820a50637778RxCUI 1111339UNII 2XG66W44KFUPC 0316571882052
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

N416571088205 followed by a unit qualifier and the quantity

Package 16571-0882-05. 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 4, 2025.

Indications (excerpt from the label)

USE(S) temporarily relieves itchy and red 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)

About NDC 16571-882

What is NDC 16571-882?: 16571-882 is the product NDC for olopatadine hydrochloride, Olopatadine hydrochloride 1 mg/mL solution, listed with the FDA by Rising Pharma Holdings, Inc.. 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?: Rising Pharma Holdings, Inc., NDC labeler code 16571. 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 Hydrochlorideolopatadine hydrochloride ophthalmic solution	Olopatadine hydrochloride 1 mg/mL	Solution/ dropsOphthalmic	RUGBY LABORATORIES	0536-1445	00536-1445-40

All 64 olopatadine hydrochloride NDCs