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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 076702
Company: MYLAN
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
OXYBUTYNIN CHLORIDE OXYBUTYNIN CHLORIDE 5MG TABLET, EXTENDED RELEASE;ORAL Discontinued None No No
Original Approvals or Tentative Approvals
Action Date Submission Action Type Submission Classification Review Priority; Orphan Status Letters, Reviews, Labels, Patient Package Insert Notes Url
11/09/2006 ORIG-1 Approval Letter (PDF)
Review (PDF)

Label is not available on this site.

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2006/076702s000LTR.pdf https://www.accessdata.fda.gov/drugsatfda_docs/anda/2006/076702Orig1s000.pdf
Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
08/19/2019 SUPPL-16 Labeling-Package Insert

Label is not available on this site.

08/19/2019 SUPPL-15 Labeling-Package Insert

Label is not available on this site.

01/22/2016 SUPPL-13 Labeling-Package Insert

Label is not available on this site.

01/22/2016 SUPPL-12 Labeling-Package Insert

Label is not available on this site.

07/26/2013 SUPPL-11 Labeling-Package Insert

Label is not available on this site.

04/29/2013 SUPPL-10 Labeling-Package Insert

Label is not available on this site.

03/01/2011 SUPPL-9 Labeling-Container/Carton Labels, Labeling-Package Insert

Label is not available on this site.

03/19/2009 SUPPL-7 Labeling

Label is not available on this site.

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