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General MedicationsOPHTHALMICGeneric

PREDAIR FORTE

PREDNISOLONE SODIUM PHOSPHATE

Standard Dose
EQ 0.9% PHOSPHATE
Max Dose
Refer to approved labeling
Primary Use
Marketing status: Discontinued
Summary

Approval overview PREDAIR FORTE is listed in Drugs@FDA under application 088165 (ANDA).

Marketing status: Discontinued Active ingredient PREDNISOLONE SODIUM PHOSPHATE Form and strength SOLUTION/DROPS;OPHTHALMIC - EQ 0.9% PHOSPHATE Sponsor PHARMAFAIR Submission history See approval history documents.

Structured Monograph

Clinical summary

Approval overview PREDAIR FORTE is listed in Drugs@FDA under application 088165 (ANDA). Marketing status: Discontinued Active ingredient PREDNISOLONE SODIUM PHOSPHATE Form and strength SOLUTION/DROPS;OPHTHALMIC - EQ 0.9% PHOSPHATE Sponsor PHARMAFAIR Submission history See approval history documents.

Monitoring

  • • Marketing status: Discontinued

Interaction Notes

  • No interaction notes stored yet.
PREDAIR FORTE (PREDNISOLONE SODIUM PHOSPHATE) | Drug Monograph | MedicHelpline