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General MedicationsTOPICALGeneric

HIBICLENS

CHLORHEXIDINE GLUCONATE

Standard Dose
4% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 HIBICLENS is listed in Drugs@FDA under application 018423 (NDA).

Review priority: STANDARD Marketing status: Discontinued Active ingredient CHLORHEXIDINE GLUCONATE Form and strength SPONGE;TOPICAL - 4% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor MOLNLYCKE HLTH Submission history Latest submission status date: 2001-12-12 00:00:00.

Structured Monograph

Clinical summary

Approval overview HIBICLENS is listed in Drugs@FDA under application 018423 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient CHLORHEXIDINE GLUCONATE Form and strength SPONGE;TOPICAL - 4% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor MOLNLYCKE HLTH Submission history Latest submission status date: 2001-12-12 00:00:00. Submission type: SUPPL.

Monitoring

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

Interaction Notes

  • No interaction notes stored yet.