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General MedicationsORALGeneric

PREDNISOLONE

PREDNISOLONE

Standard Dose
1MG
Max Dose
Refer to approved labeling
Primary Use
Marketing status: Discontinued
Summary

Approval overview PREDNISOLONE is listed in Drugs@FDA under application 084439 (ANDA).

Marketing status: Discontinued Active ingredient PREDNISOLONE Form and strength TABLET;ORAL - 1MG Sponsor EVERYLIFE Submission history Latest submission status date: 1975-05-20 00:00:00.

Structured Monograph

Clinical summary

Approval overview PREDNISOLONE is listed in Drugs@FDA under application 084439 (ANDA). Marketing status: Discontinued Active ingredient PREDNISOLONE Form and strength TABLET;ORAL - 1MG Sponsor EVERYLIFE Submission history Latest submission status date: 1975-05-20 00:00:00. Submission type: ORIG.

Monitoring

  • • Marketing status: Discontinued

Interaction Notes

  • No interaction notes stored yet.