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Sulfacetamide Sodium and Prednisolone Sodium Phosphate

NDC 68071-1650 · HUMAN PRESCRIPTION DRUG · SOLUTION/ DROPS

Labeler / ManufacturerNuCare Pharmaceuticals,Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA074449
Dosage form / routeSOLUTION/ DROPS · OPHTHALMIC
Active ingredientsPREDNISOLONE SODIUM PHOSPHATE (2.3 mg/mL)
SULFACETAMIDE SODIUM (100 mg/mL)
Marketing started19951229
Package count1

External sources

Source: openFDA. Public-domain (CC0).