Drugs@FDA: FDA-Approved Drugs
Company: AUROBINDO PHARMA LTD
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
---|---|---|---|---|---|---|---|
DIVALPROEX SODIUM | DIVALPROEX SODIUM | EQ 250MG VALPROIC ACID | TABLET, EXTENDED RELEASE;ORAL | Prescription | AB | No | No |
DIVALPROEX SODIUM | DIVALPROEX SODIUM | EQ 500MG 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 |
---|---|---|---|---|---|---|---|
06/02/2014 | 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 |
---|---|---|---|---|---|
06/03/2024 | SUPPL-29 | Labeling-Medication Guide, Labeling-Package Insert |
Label is not available on this site. |
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07/11/2023 | SUPPL-27 | Labeling-Medication Guide, Labeling-Package Insert |
Label is not available on this site. |
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12/27/2022 | SUPPL-25 | Labeling-Package Insert, Labeling-Medication Guide |
Label is not available on this site. |
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12/27/2022 | SUPPL-22 | Labeling-Medication Guide, Labeling-Package Insert |
Label is not available on this site. |
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02/10/2020 | SUPPL-21 | Labeling-Medication Guide, Labeling-Package Insert |
Label is not available on this site. |
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02/10/2020 | SUPPL-20 | Labeling-Package Insert, Labeling-Medication Guide |
Label is not available on this site. |
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02/10/2020 | SUPPL-17 | Labeling-Medication Guide, Labeling-Package Insert |
Label is not available on this site. |
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02/10/2020 | SUPPL-16 | Labeling-Package Insert |
Label is not available on this site. |
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02/10/2020 | SUPPL-14 | Labeling-Package Insert |
Label is not available on this site. |
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02/10/2020 | SUPPL-13 | Labeling-Medication Guide, Labeling-Patient Package Insert |
Label is not available on this site. |
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02/10/2020 | SUPPL-11 | Labeling-Package Insert, Labeling-Medication Guide |
Label is not available on this site. |
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02/10/2020 | SUPPL-10 | Labeling-Package Insert |
Label is not available on this site. |
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02/10/2020 | SUPPL-9 | Labeling-Package Insert |
Label is not available on this site. |
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09/23/2015 | SUPPL-7 | Labeling-Container/Carton Labels, Labeling-Package Insert |
Label is not available on this site. |
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09/23/2015 | SUPPL-5 | Labeling-Package Insert |
Label is not available on this site. |
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09/23/2015 | SUPPL-4 | Labeling-Package Insert |
Label is not available on this site. |
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11/20/2014 | SUPPL-3 | Labeling-Package Insert |
Label is not available on this site. |
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11/20/2014 | SUPPL-2 | Labeling-Package Insert |
Label is not available on this site. |
DIVALPROEX SODIUM
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 | 215527 | ANNORA PHARMA |
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 |
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 | 215527 | ANNORA PHARMA |
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 |