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General MedicationsORALGeneric

IBUPROFEN AND FAMOTIDINE

FAMOTIDINE; IBUPROFEN

Standard Dose
26.6MG;800MG
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: Discontinued
Summary

Approval overview IBUPROFEN AND FAMOTIDINE is listed in Drugs@FDA under application 219538 (ANDA).

Review priority: STANDARD Marketing status: Discontinued Active ingredient FAMOTIDINE; IBUPROFEN Form and strength TABLET;ORAL - 26.6MG;800MG Sponsor AUROBINDO PHARMA LTD Submission history Latest submission status date: 2025-06-30 00:00:00.

Structured Monograph

Clinical summary

Approval overview IBUPROFEN AND FAMOTIDINE is listed in Drugs@FDA under application 219538 (ANDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient FAMOTIDINE; IBUPROFEN Form and strength TABLET;ORAL - 26.6MG;800MG Sponsor AUROBINDO PHARMA LTD Submission history Latest submission status date: 2025-06-30 00:00:00. Submission type: ORIG.

Monitoring

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

Interaction Notes

  • No interaction notes stored yet.