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
0574-4135_1c88bd5e-7e65-4cfe-b1d9-0894f4a4f82a
Product NDC
0574-4135
Form
SUSPENSION/ DROPS
Composition / generic term
loteprednol etabonate
Labeler
Padagis US LLC
Marketing category
ANDA
Marketing start / end (source format)
20260112
Source listing expiry
20271231

Source-listed ingredients

  • LOTEPREDNOL ETABONATE — 5 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE, DROPPER in 1 CARTON (0574-4135-05) / 5 mL in 1 BOTTLE, DROPPER · 0574-4135-05
  • 1 BOTTLE, DROPPER in 1 CARTON (0574-4135-10) / 10 mL in 1 BOTTLE, DROPPER · 0574-4135-10
  • 1 BOTTLE, DROPPER in 1 CARTON (0574-4135-15) / 15 mL in 1 BOTTLE, DROPPER · 0574-4135-15

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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