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Depakote
Depakote - 0074-6114-71 - (Divalproex Sodium)
Drug Information of Depakote
| Product NDC: | 0074-6114 |
| 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: | 0074-6114 |
| Labeler Name: | AbbVie Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019680 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19890912 |
Package Information of Depakote
| Package NDC: | 0074-6114-71 |
| Package Description: | 6 BLISTER PACK in 1 CARTON (0074-6114-71) > 6 CAPSULE in 1 BLISTER PACK |
NDC Information of Depakote
| NDC Code | 0074-6114-71 |
| Proprietary Name | Depakote |
| Package Description | 6 BLISTER PACK in 1 CARTON (0074-6114-71) > 6 CAPSULE in 1 BLISTER PACK |
| Product NDC | 0074-6114 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Divalproex Sodium |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 19890912 |
| Marketing Category Name | NDA |
| Labeler Name | AbbVie Inc. |
| 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] |
