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General MedicationsORALGeneric

CHILDREN'S ALLEGRA ALLERGY

FEXOFENADINE HYDROCHLORIDE

Standard Dose
30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: Discontinued
Summary

Approval overview CHILDREN'S ALLEGRA ALLERGY is listed in Drugs@FDA under application 020872 (NDA).

Review priority: STANDARD Marketing status: Discontinued Active ingredient FEXOFENADINE HYDROCHLORIDE Form and strength TABLET;ORAL - 30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor CHATTEM SANOFI Submission history Latest submission status date: 2023-08-01 00:00:00.

Structured Monograph

Clinical summary

Approval overview CHILDREN'S ALLEGRA ALLERGY is listed in Drugs@FDA under application 020872 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient FEXOFENADINE HYDROCHLORIDE Form and strength TABLET;ORAL - 30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor CHATTEM SANOFI Submission history Latest submission status date: 2023-08-01 00:00:00. Submission type: SUPPL.

Monitoring

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

Interaction Notes

  • No interaction notes stored yet.
CHILDREN'S ALLEGRA ALLERGY (FEXOFENADINE HYDROCHLORIDE) | Drug Monograph | MedicHelpline