United States · FDA National Drug Code directory

LOTEPREDNOL ETABONATE

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
60219-1362_0e87ba50-9918-4733-8ed3-95ce3c772b07
Product NDC
60219-1362
Form
SUSPENSION/ DROPS
Composition / generic term
loteprednol etabonate
Labeler
Amneal Pharmaceuticals NY LLC
Marketing category
ANDA
Marketing start / end (source format)
20250522
Source listing expiry
20261231

Source-listed ingredients

  • LOTEPREDNOL ETABONATE — 5 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE in 1 CARTON (60219-1362-1) / 5 mL in 1 BOTTLE · 60219-1362-1
  • 1 BOTTLE in 1 CARTON (60219-1362-2) / 10 mL in 1 BOTTLE · 60219-1362-2
  • 1 BOTTLE in 1 CARTON (60219-1362-3) / 15 mL in 1 BOTTLE · 60219-1362-3

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 →