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General MedicationsOPHTHALMICGeneric

PREDSULFAIR II

PREDNISOLONE ACETATE; SULFACETAMIDE SODIUM

Standard Dose
0.2%;10%
Max Dose
Refer to approved labeling
Primary Use
Marketing status: Discontinued
Summary

Approval overview PREDSULFAIR II is listed in Drugs@FDA under application 088837 (ANDA).

Marketing status: Discontinued Active ingredient PREDNISOLONE ACETATE; SULFACETAMIDE SODIUM Form and strength SUSPENSION/DROPS;OPHTHALMIC - 0.2%;10% Sponsor PHARMAFAIR Submission history See approval history documents.

Structured Monograph

Clinical summary

Approval overview PREDSULFAIR II is listed in Drugs@FDA under application 088837 (ANDA). Marketing status: Discontinued Active ingredient PREDNISOLONE ACETATE; SULFACETAMIDE SODIUM Form and strength SUSPENSION/DROPS;OPHTHALMIC - 0.2%;10% Sponsor PHARMAFAIR Submission history See approval history documents.

Monitoring

  • • Marketing status: Discontinued

Interaction Notes

  • No interaction notes stored yet.