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
0536-1307_ebf26e25-d073-ca39-6b0b-dec0fa2c2107
Product NDC
0536-1307
Form
SOLUTION/ DROPS
Composition / generic term
Olopatadine Hydrochloride
Labeler
Rugby Laboratories
Marketing category
ANDA
Marketing start / end (source format)
20210115
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, DROPPER in 1 CARTON (0536-1307-23) / 2.5 mL in 1 BOTTLE, DROPPER · 0536-1307-23

Source and coverage

Open FDA National Drug Code directory

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.

Browse United States records →
Olopatadine Hydrochloride — United States | Molindra Medicines