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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 207113
Company: ACTAVIS LABS FL INC
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE 325MG; 7.5MG TABLET, EXTENDED RELEASE;ORAL None (Tentative Approval) 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
09/27/2016 ORIG-1 Tentative Approval STANDARD Letter (PDF)

Label is not available on this site.

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2016/207113Orig1s000TAltr.pdf
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