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Depakote
Depakote - 54868-1208-6 - (divalproex sodium)
Drug Information of Depakote
| Product NDC: | 54868-1208 |
| Proprietary Name: | Depakote |
| Non Proprietary Name: | divalproex sodium |
| Active Ingredient(s): | 250 mg/1 & nbsp; divalproex sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, DELAYED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Depakote
| Product NDC: | 54868-1208 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018723 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19960213 |
Package Information of Depakote
| Package NDC: | 54868-1208-6 |
| Package Description: | 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (54868-1208-6) |
NDC Information of Depakote
| NDC Code | 54868-1208-6 |
| Proprietary Name | Depakote |
| Package Description | 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (54868-1208-6) |
| Product NDC | 54868-1208 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | divalproex sodium |
| Dosage Form Name | TABLET, DELAYED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 19960213 |
| Marketing Category Name | NDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | DIVALPROEX SODIUM |
| Strength Number | 250 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC] |
