| NDC Code | 68084-317-01 |
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| Package Description | 10 BLISTER PACK in 1 CARTON (68084-317-01) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68084-317-11) |
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| Product NDC | 68084-317 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Divalproex Sodium Extended-release |
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| Non-Proprietary Name | Divalproex Sodium Extended-release |
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| Dosage Form | TABLET, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20091014 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA078705 |
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| Manufacturer | American Health Packaging |
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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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