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
70748-300_822adc09-88c3-41fa-922a-66dfa7e412b2
Product NDC
70748-300
Form
SUSPENSION
Composition / generic term
loteprednol etabonate
Labeler
Lupin Pharmaceuticals, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20250715
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 in 1 CARTON (70748-300-01) / 5 mL in 1 BOTTLE · 70748-300-01
  • 1 BOTTLE in 1 CARTON (70748-300-02) / 10 mL in 1 BOTTLE · 70748-300-02

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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