United States · FDA National Drug Code directory
Olopatadine Hydrochloride
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
- 73581-712_598156e4-f184-86f5-e063-6294a90a64df
- Product NDC
- 73581-712
- Form
- SOLUTION
- Composition / generic term
- Olopatadine Hydrochloride
- Labeler
- YYBA CORP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260831
- Source listing expiry
- 20271231
Source-listed ingredients
- OLOPATADINE HYDROCHLORIDE — 2 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 2 BOTTLE in 1 CARTON (73581-712-02) / 2.5 mL in 1 BOTTLE · 73581-712-02
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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