NDC codes

FDA NDC Directory
Product NDC (as listed)50090-7959Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-7959Add 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 NDC11-digit (billing)PackageCopy
50090-7959-0500907959001 BOTTLE, PLASTIC in 1 CARTON (50090-7959-0) / 5 mL in 1 BOTTLE, PLASTICMarketed from May 5, 2026

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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
Generic name (nonproprietary)
olopatadine
Active ingredients
Olopatadine hydrochloride — 1 mg/mL
Dosage form
Solution/ drops
Route
Ophthalmic
Labeler
A-S Medication SolutionsNDC labeler code 50090
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 206306
Marketing start
Listing expires
Other FDA classes
Decreased Histamine Release (Physiologic effect)Histamine H1 Receptor Antagonists (Mechanism)
Identifiers
Product ID 50090-7959_edfacea9-790d-4adc-8cc4-fed868dc2cc7SPL ID edfacea9-790d-4adc-8cc4-fed868dc2cc7SPL set ID ef573cb9-7829-4bcb-9e4c-b26014cd94dbRxCUI 1111339UNII 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. Ophthalmic products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N450090795900 followed by a unit qualifier and the quantity

Package 50090-7959-00. 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 .

Indications (excerpt from the label)

Use 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 50090-7959

What is NDC 50090-7959?
50090-7959 is the product NDC for Olopatadine, Olopatadine hydrochloride 1 mg/mL solution/ drops, listed with the FDA by A-S Medication Solutions. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Olopatadine.
What is the active ingredient?
Olopatadine hydrochloride.
Who is the labeler?
A-S Medication Solutions, NDC labeler code 50090. 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?
1 other product NDC are listed under this name. See all Olopatadine 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 NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
OlopatadineOlopatadine hydrochloride 1 mg/mLSolution/ dropsOphthalmicSomerset Therapeutics, LLC70069-01770069-0017-01

Other NDCs under ANDA 206306

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

FDA NDC Directory listings under ANDA 206306
ProductStrengthForm · routeLabelerProduct NDC
OlopatadineOlopatadine hydrochloride 1 mg/mLSolution/ dropsOphthalmicSomerset Therapeutics, LLC70069-017

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