United States · FDA National Drug Code directory
Difluprednate Ophthalmic
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
- 0781-6000_a0888296-a4c5-4392-a2a9-98770f6b179a
- Product NDC
- 0781-6000
- Form
- EMULSION
- Composition / generic term
- Difluprednate Ophthalmic
- Labeler
- Sandoz Inc
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start / end (source format)
- 20130515
- Source listing expiry
- 20271231
Source-listed ingredients
- DIFLUPREDNATE — .5 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (0781-6000-78) / 5 mL in 1 BOTTLE · 0781-6000-78
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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