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Depakote
Depakote - 55154-0113-0 - (divalproex sodium)
Drug Information of Depakote
| Product NDC: | 55154-0113 |
| Proprietary Name: | Depakote |
| Non Proprietary Name: | divalproex sodium |
| Active Ingredient(s): | 125 mg/1 & nbsp; divalproex sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Depakote
| Product NDC: | 55154-0113 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019680 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100607 |
Package Information of Depakote
| Package NDC: | 55154-0113-0 |
| Package Description: | 10 BLISTER PACK in 1 BAG (55154-0113-0) > 1 CAPSULE in 1 BLISTER PACK |
NDC Information of Depakote
| NDC Code | 55154-0113-0 |
| Proprietary Name | Depakote |
| Package Description | 10 BLISTER PACK in 1 BAG (55154-0113-0) > 1 CAPSULE in 1 BLISTER PACK |
| Product NDC | 55154-0113 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | divalproex sodium |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20100607 |
| Marketing Category Name | NDA |
| Labeler Name | Cardinal Health |
| Substance Name | DIVALPROEX SODIUM |
| Strength Number | 125 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC] |
