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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 078705
Company: WOCKHARDT
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
DIVALPROEX SODIUM DIVALPROEX SODIUM EQ 500MG VALPROIC ACID TABLET, EXTENDED RELEASE;ORAL Prescription AB No No
DIVALPROEX SODIUM DIVALPROEX SODIUM EQ 250MG VALPROIC ACID TABLET, EXTENDED RELEASE;ORAL Prescription AB 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
02/10/2009 ORIG-1 Approval Review (PDF)

Label is not available on this site.

https://www.accessdata.fda.gov/drugsatfda_docs/anda/2009/078705Orig1s000.pdf
Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
11/08/2014 SUPPL-6 Labeling-Medication Guide, Labeling-Package Insert

Label is not available on this site.

11/08/2014 SUPPL-5 Labeling-Package Insert

Label is not available on this site.

08/05/2009 SUPPL-4 Labeling

Label is not available on this site.

08/04/2009 SUPPL-3 Labeling

Label is not available on this site.

08/04/2009 SUPPL-2

Label is not available on this site.

08/04/2009 SUPPL-1

Label is not available on this site.

DIVALPROEX SODIUM

TABLET, EXTENDED RELEASE;ORAL; EQ 500MG VALPROIC ACID
TE Code = AB

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
DEPAKOTE ER DIVALPROEX SODIUM EQ 500MG VALPROIC ACID TABLET, EXTENDED RELEASE;ORAL Prescription Yes AB 021168 ABBVIE
DIVALPROEX SODIUM DIVALPROEX SODIUM EQ 500MG VALPROIC ACID TABLET, EXTENDED RELEASE;ORAL Prescription No AB 203730 AMNEAL PHARMS
DIVALPROEX SODIUM DIVALPROEX SODIUM EQ 500MG VALPROIC ACID TABLET, EXTENDED RELEASE;ORAL Prescription No AB 202419 AUROBINDO PHARMA LTD
DIVALPROEX SODIUM DIVALPROEX SODIUM EQ 500MG VALPROIC ACID TABLET, EXTENDED RELEASE;ORAL Prescription No AB 209286 LUPIN LTD
DIVALPROEX SODIUM DIVALPROEX SODIUM EQ 500MG VALPROIC ACID TABLET, EXTENDED RELEASE;ORAL Prescription No AB 077567 MYLAN
DIVALPROEX SODIUM DIVALPROEX SODIUM EQ 500MG VALPROIC ACID TABLET, EXTENDED RELEASE;ORAL Prescription No AB 090070 REDDYS
DIVALPROEX SODIUM DIVALPROEX SODIUM EQ 500MG VALPROIC ACID TABLET, EXTENDED RELEASE;ORAL Prescription No AB 214643 UNICHEM
DIVALPROEX SODIUM DIVALPROEX SODIUM EQ 500MG VALPROIC ACID TABLET, EXTENDED RELEASE;ORAL Prescription No AB 078705 WOCKHARDT
DIVALPROEX SODIUM DIVALPROEX SODIUM EQ 500MG VALPROIC ACID TABLET, EXTENDED RELEASE;ORAL Prescription No AB 078239 ZYDUS PHARMS USA INC

TABLET, EXTENDED RELEASE;ORAL; EQ 250MG VALPROIC ACID
TE Code = AB

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
DEPAKOTE ER DIVALPROEX SODIUM EQ 250MG VALPROIC ACID TABLET, EXTENDED RELEASE;ORAL Prescription Yes AB 021168 ABBVIE
DIVALPROEX SODIUM DIVALPROEX SODIUM EQ 250MG VALPROIC ACID TABLET, EXTENDED RELEASE;ORAL Prescription No AB 203730 AMNEAL PHARMS
DIVALPROEX SODIUM DIVALPROEX SODIUM EQ 250MG VALPROIC ACID TABLET, EXTENDED RELEASE;ORAL Prescription No AB 202419 AUROBINDO PHARMA LTD
DIVALPROEX SODIUM DIVALPROEX SODIUM EQ 250MG VALPROIC ACID TABLET, EXTENDED RELEASE;ORAL Prescription No AB 090161 DR REDDYS LABS LTD
DIVALPROEX SODIUM DIVALPROEX SODIUM EQ 250MG VALPROIC ACID TABLET, EXTENDED RELEASE;ORAL Prescription No AB 209286 LUPIN LTD
DIVALPROEX SODIUM DIVALPROEX SODIUM EQ 250MG VALPROIC ACID TABLET, EXTENDED RELEASE;ORAL Prescription No AB 077567 MYLAN
DIVALPROEX SODIUM DIVALPROEX SODIUM EQ 250MG VALPROIC ACID TABLET, EXTENDED RELEASE;ORAL Prescription No AB 214643 UNICHEM
DIVALPROEX SODIUM DIVALPROEX SODIUM EQ 250MG VALPROIC ACID TABLET, EXTENDED RELEASE;ORAL Prescription No AB 078705 WOCKHARDT
DIVALPROEX SODIUM DIVALPROEX SODIUM EQ 250MG VALPROIC ACID TABLET, EXTENDED RELEASE;ORAL Prescription No AB 078239 ZYDUS PHARMS USA INC
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