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FDA ANDA · ANDA202332

OXYBUTYNIN

Sponsor: ZYDUS PHARMS

APPLICATION
ANDA202332
TYPE
ANDA
ORIGINAL APPROVAL
2017-06-26
LATEST ACTION
2021-10-18
ROUTE
ORAL
DOSAGE FORM
TABLET, EXTENDED RELEASE
MARKETING STATUS
Prescription

Products

OXYBUTYNIN CHLORIDEPrescription
OXYBUTYNIN CHLORIDE 15MG · TABLET, EXTENDED RELEASE · ORAL
OXYBUTYNIN CHLORIDEPrescription
OXYBUTYNIN CHLORIDE 5MG · TABLET, EXTENDED RELEASE · ORAL
OXYBUTYNIN CHLORIDEPrescription
OXYBUTYNIN CHLORIDE 10MG · TABLET, EXTENDED RELEASE · ORAL

Approval history

2021-10-18Labeling · Supplement 7 · standardAP
2020-02-28Labeling · Supplement 4 · standardAP
2019-08-19Labeling · Supplement 3 · standardAP
2017-06-26OriginalAP
VIEW ON DRUGS@FDA ↗

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Source: FDA Drugs@FDA. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data, not medical, legal, or regulatory advice.

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