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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 205102
Company: SECAN PHARMS
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
LEVETIRACETAM LEVETIRACETAM 250MG TABLET;ORAL None (Tentative Approval) None No No
LEVETIRACETAM LEVETIRACETAM 750MG TABLET;ORAL None (Tentative Approval) None No No
LEVETIRACETAM LEVETIRACETAM 1GM TABLET;ORAL Discontinued None No No
LEVETIRACETAM LEVETIRACETAM 500MG 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
12/16/2015 ORIG-3 Tentative Approval STANDARD

Label is not available on this site.

12/16/2015 ORIG-2 Approval STANDARD

Label is not available on this site.

12/16/2015 ORIG-1 Approval STANDARD Letter (PDF)

Label is not available on this site.

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2021/205102Orig1s000Correctedltr.pdf
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