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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 090601
Company: HIKMA
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
LEVETIRACETAM LEVETIRACETAM 100MG/ML SOLUTION;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
02/28/2012 ORIG-1 Approval

Label is not available on this site.

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
08/05/2022 SUPPL-10 Labeling-Medication Guide, Labeling-Package Insert

Label is not available on this site.

08/05/2022 SUPPL-6 Labeling-Package Insert

Label is not available on this site.

08/05/2022 SUPPL-5 Labeling-Medication Guide, Labeling-Package Insert

Label is not available on this site.

12/01/2015 SUPPL-4 Labeling-Container/Carton Labels

Label is not available on this site.

12/01/2015 SUPPL-2 Labeling-Package Insert

Label is not available on this site.

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