United States · FDA National Drug Code directory

Olopatadine Hcl

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
70512-520_45728450-eb13-7314-e063-6394a90ae6d1
Product NDC
70512-520
Form
SOLUTION/ DROPS
Composition / generic term
Olopatadine Hcl
Labeler
Sola Pharmaceuticals
Marketing category
ANDA
Marketing start / end (source format)
20220705
Source listing expiry
20261231

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 (70512-520-05) / 5 mL in 1 BOTTLE, PLASTIC · 70512-520-05

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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