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DIVALPROEX SODIUM
DIVALPROEX SODIUM - 55648-724-04 - (DIVALPROEX SODIUM)
Drug Information of DIVALPROEX SODIUM
| Product NDC: | 55648-724 |
| Proprietary Name: | DIVALPROEX SODIUM |
| Non Proprietary Name: | DIVALPROEX SODIUM |
| Active Ingredient(s): | 250 mg/1 & nbsp; DIVALPROEX SODIUM |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DIVALPROEX SODIUM
| Product NDC: | 55648-724 |
| Labeler Name: | WOCKHARDT LIMITED |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078705 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090210 |
Package Information of DIVALPROEX SODIUM
| Package NDC: | 55648-724-04 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (55648-724-04) > 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
NDC Information of DIVALPROEX SODIUM
| NDC Code | 55648-724-04 |
| Proprietary Name | DIVALPROEX SODIUM |
| Package Description | 10 BLISTER PACK in 1 CARTON (55648-724-04) > 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
| Product NDC | 55648-724 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | DIVALPROEX SODIUM |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20090210 |
| Marketing Category Name | ANDA |
| Labeler Name | WOCKHARDT LIMITED |
| 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] |
