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
- 68071-1650_1d4de4f7-e86f-d269-e063-6294a90ab688
- Product NDC
- 68071-1650
- Form
- SOLUTION/ DROPS
- Composition / generic term
- Sulfacetamide Sodium and Prednisolone Sodium Phosphate
- Labeler
- NuCare Pharmaceuticals,Inc.
- 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
- 5 mL in 1 BOX (68071-1650-5) · 68071-1650-5
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 →