| NDC Code | 0115-6922-19 |
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| Package Description | 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-6922-19) |
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| Product NDC | 0115-6922 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Divalproex Sodium |
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| Non-Proprietary Name | Divalproex Sodium |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20090804 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA078791 |
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| Manufacturer | Global Pharmaceuticals, Division of Impax Laboratories Inc. |
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| Substance Name | DIVALPROEX SODIUM |
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| Strength | 500 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC] |
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