United States · FDA National Drug Code directory
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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
- 0065-8150_7f324d32-7a86-4976-b0f4-b80283e5fc29
- Product NDC
- 0065-8150
- Form
- SOLUTION
- Composition / generic term
- OLOPATADINE HYDROCHLORIDE
- Labeler
- Alcon Laboratories, Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20200228
- Source listing expiry
- 20271231
Source-listed ingredients
- OLOPATADINE HYDROCHLORIDE — 2 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, PLASTIC in 1 CARTON (0065-8150-01) / 2.5 mL in 1 BOTTLE, PLASTIC · 0065-8150-01
- 2 BOTTLE, PLASTIC in 1 CARTON (0065-8150-03) / 2.5 mL in 1 BOTTLE, PLASTIC · 0065-8150-03
- 1 BOTTLE, PLASTIC in 1 CARTON (0065-8150-04) / .5 mL in 1 BOTTLE, PLASTIC · 0065-8150-04
- 3 BOTTLE, PLASTIC in 1 CARTON (0065-8150-07) / 2.5 mL in 1 BOTTLE, PLASTIC · 0065-8150-07
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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