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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 090407
Company: RISING
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
DIVALPROEX SODIUM DIVALPROEX SODIUM EQ 125MG VALPROIC ACID CAPSULE, DELAYED REL PELLETS;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
03/28/2011 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
06/25/2020 SUPPL-14 Labeling-Medication Guide, Labeling-Package Insert

Label is not available on this site.

06/25/2020 SUPPL-13 Labeling-Medication Guide, Labeling-Package Insert

Label is not available on this site.

06/25/2020 SUPPL-12 Labeling-Package Insert

Label is not available on this site.

06/25/2020 SUPPL-11 Labeling-Package Insert

Label is not available on this site.

06/25/2020 SUPPL-10 Labeling-Package Insert

Label is not available on this site.

06/25/2020 SUPPL-9 Labeling-Medication Guide, Labeling-Package Insert

Label is not available on this site.

06/25/2020 SUPPL-8 Labeling-Package Insert

Label is not available on this site.

12/08/2014 SUPPL-6 Labeling-Package Insert

Label is not available on this site.

12/30/2013 SUPPL-5 Labeling-Package Insert

Label is not available on this site.

12/30/2013 SUPPL-2 Labeling-Container/Carton Labels, Labeling-Package Insert

Label is not available on this site.

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