# Sulfacetamide Sodium and Prednisolone Sodium Phosphate

NDC: 68071-1650
Generic name: Sulfacetamide Sodium and Prednisolone Sodium Phosphate
Labeler / Manufacturer: NuCare Pharmaceuticals,Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION/ DROPS
Routes: OPHTHALMIC
Marketing started: 19951229

FDA application: ANDA074449

## Active ingredients

- PREDNISOLONE SODIUM PHOSPHATE: 2.3 mg/mL
- SULFACETAMIDE SODIUM: 100 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68071-1650"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68071-1650
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=835def0b-ed5a-61a0-e053-2a91aa0ae7ae