United States · FDA National Drug Code directory
Olopatadine
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 50090-7959_edfacea9-790d-4adc-8cc4-fed868dc2cc7
- Product NDC
- 50090-7959
- Form
- SOLUTION/ DROPS
- Composition / generic term
- Olopatadine
- Labeler
- A-S Medication Solutions
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240415
- Source listing expiry
- 20271231
Source-listed ingredients
- OLOPATADINE HYDROCHLORIDE — 1 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, PLASTIC in 1 CARTON (50090-7959-0) / 5 mL in 1 BOTTLE, PLASTIC · 50090-7959-0
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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