| NDC Code | 68382-134-16 |
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| Package Description | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-134-16) |
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| Product NDC | 68382-134 |
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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 | 20130107 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA078239 |
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| Manufacturer | Zydus Pharmaceuticals USA 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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