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General MedicationsORALGeneric

FENOPROFEN CALCIUM

FENOPROFEN CALCIUM

Standard Dose
EQ 600MG BASE
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: Discontinued
Summary

Approval overview FENOPROFEN CALCIUM is listed in Drugs@FDA under application 072902 (ANDA).

Review priority: STANDARD Marketing status: Discontinued Active ingredient FENOPROFEN CALCIUM Form and strength TABLET;ORAL - EQ 600MG BASE Sponsor SUN PHARM INDUSTRIES Submission history Latest submission status date: 2024-11-21 00:00:00.

Structured Monograph

Clinical summary

Approval overview FENOPROFEN CALCIUM is listed in Drugs@FDA under application 072902 (ANDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient FENOPROFEN CALCIUM Form and strength TABLET;ORAL - EQ 600MG BASE Sponsor SUN PHARM INDUSTRIES Submission history Latest submission status date: 2024-11-21 00:00:00. Submission type: SUPPL.

Monitoring

  • • Marketing status: Discontinued
  • • Review priority: STANDARD

Interaction Notes

  • No interaction notes stored yet.