United States · FDA National Drug Code directory
Sulfacetamide Sodium and Prednisolone Sodium Phosphate
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
- 24208-317_06ea3d35-67bf-d0b8-e063-6294a90a5b0c
- Product NDC
- 24208-317
- Form
- SOLUTION/ DROPS
- Composition / generic term
- Sulfacetamide Sodium and Prednisolone Sodium Phosphate
- Labeler
- Bausch & Lomb Incoporated
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19951229
- Source listing expiry
- 20261231
Source-listed ingredients
- SULFACETAMIDE SODIUM — 100 mg/mL
- PREDNISOLONE SODIUM PHOSPHATE — 2.3 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, DROPPER in 1 CARTON (24208-317-05) / 5 mL in 1 BOTTLE, DROPPER · 24208-317-05
- 1 BOTTLE, DROPPER in 1 CARTON (24208-317-10) / 10 mL in 1 BOTTLE, DROPPER · 24208-317-10
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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