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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 204005
Company: MYLAN
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
LAMIVUDINE AND ZIDOVUDINE LAMIVUDINE; ZIDOVUDINE 150MG;300MG TABLET;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
08/28/2014 ORIG-1 Approval Letter (PDF)

Label is not available on this site.

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2014/204005Orig1s000ltr.pdf
Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
08/27/2019 SUPPL-9 Labeling-Package Insert

Label is not available on this site.

08/27/2019 SUPPL-8 Labeling-Package Insert

Label is not available on this site.

08/27/2019 SUPPL-7 Labeling-Package Insert

Label is not available on this site.

08/27/2019 SUPPL-6 Labeling-Package Insert

Label is not available on this site.

08/27/2019 SUPPL-2 Labeling-Package Insert

Label is not available on this site.

04/16/2015 SUPPL-1 Labeling-Package Insert

Label is not available on this site.

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