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General MedicationsORALStandard

Oxybutynin Chloride

Oxybutynin Chloride

Standard Dose
15 MG.
Max Dose
Refer to approved labeling
Primary Use
Marketing status: Prescription
Summary

Approval overview Oxybutynin Chloride is listed in Drugs@FDA under application 078293 (ANDA).

Marketing status: Prescription Active ingredient Oxybutynin Chloride Form and strength TABLET, EXTENDED RELEASE; ORAL - 15 MG.

Structured Monograph

Clinical summary

Approval overview Oxybutynin Chloride is listed in Drugs@FDA under application 078293 (ANDA). Marketing status: Prescription Active ingredient Oxybutynin Chloride Form and strength TABLET, EXTENDED RELEASE; ORAL - 15 MG. Sponsor MYLAN PHARMS INC Submission history Latest submission status date: 2007-05-10 00:00:00. Submission type: ORIG.

Monitoring

  • • Marketing status: Prescription

Interaction Notes

  • No interaction notes stored yet.