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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 202095
Company: LOTUS PHARM CO LTD
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
LEVETIRACETAM LEVETIRACETAM 750MG TABLET, EXTENDED RELEASE;ORAL Discontinued None No No
LEVETIRACETAM LEVETIRACETAM 500MG 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
06/06/2016 ORIG-1 Approval Not Applicable

Label is not available on this site.

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
11/10/2021 SUPPL-8 Labeling-Medication Guide, Labeling-Package Insert

Label is not available on this site.

11/10/2021 SUPPL-7 Labeling-Medication Guide, Labeling-Package Insert

Label is not available on this site.

11/10/2021 SUPPL-5 Labeling-Package Insert

Label is not available on this site.

11/10/2021 SUPPL-3 Labeling-Package Insert, Labeling-Medication Guide, Labeling-Package Insert

Label is not available on this site.

12/15/2016 SUPPL-2 Labeling-Package Insert

Label is not available on this site.

12/15/2016 SUPPL-1 Labeling-Proprietary Name Change

Label is not available on this site.

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