What is NDC 51407-663?

51407-663 is the product NDC for Olopatadine hydrochloride, Olopatadine hydrochloride 1 mg/mL solution/ drops, listed with the FDA by Golden State Medical Supply, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

Golden State Medical Supply, Inc., NDC labeler code 51407. 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 51407-663

NDC codes

FDA NDC Directory

Product NDC (as listed)51407-663Labeler and product segments. Claims need a package NDC.

Product NDC at billing width51407-0663Add 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
51407-663-05	51407066305	1 BOTTLE, PLASTIC in 1 CARTON (51407-663-05) / 5 mL in 1 BOTTLE, PLASTICMarketed from Oct 3, 2022

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/ drops
Route: Ophthalmic
Labeler: Golden State Medical Supply, Inc.NDC labeler code 51407
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 078350
Marketing start: Dec 7, 2015
Listing expires: Dec 31, 2026
Other FDA classes: Decreased Histamine Release (Physiologic effect)Histamine H1 Receptor Antagonists (Mechanism)
Identifiers: Product ID 51407-663_445f4401-cd57-82ed-e063-6394a90a1a3fSPL ID 445f4401-cd57-82ed-e063-6394a90a1a3fSPL set ID ec0c8c56-68d2-e63e-e053-2995a90a8db2RxCUI 1111339UNII 2XG66W44KFUPC 0351407663054
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

N451407066305 followed by a unit qualifier and the quantity

Package 51407-0663-05. 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 Nov 24, 2025.

Indications (excerpt from the label)

Uses 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 51407-663

What is NDC 51407-663?: 51407-663 is the product NDC for Olopatadine hydrochloride, Olopatadine hydrochloride 1 mg/mL solution/ drops, listed with the FDA by Golden State Medical Supply, 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?: Golden State Medical Supply, Inc., NDC labeler code 51407. 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

Other NDCs under ANDA 078350

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

FDA NDC Directory listings under ANDA 078350
Product	Strength	Form · route	Labeler	Product NDC
Olopatadine hydrochloride	Olopatadine hydrochloride 1 mg/mL	Solution/ dropsOphthalmic	Apotex Corp.	60505-6221
Olopatadine Hydrochloride	Olopatadine hydrochloride 1 mg/mL	Solution/ dropsOphthalmic	Allegiant Health	69168-480