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Divalproex sodium
Divalproex sodium - 55111-532-78 - (Divalproex sodium)
Drug Information of Divalproex sodium
| Product NDC: | 55111-532 |
| Proprietary Name: | Divalproex sodium |
| 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 Divalproex sodium
| Product NDC: | 55111-532 |
| Labeler Name: | Dr. Reddy's Laboratories Ltd |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078979 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090123 |
Package Information of Divalproex sodium
| Package NDC: | 55111-532-78 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (55111-532-78) > 10 CAPSULE in 1 BLISTER PACK (55111-532-79) |
NDC Information of Divalproex sodium
| NDC Code | 55111-532-78 |
| Proprietary Name | Divalproex sodium |
| Package Description | 10 BLISTER PACK in 1 CARTON (55111-532-78) > 10 CAPSULE in 1 BLISTER PACK (55111-532-79) |
| Product NDC | 55111-532 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Divalproex sodium |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20090123 |
| Marketing Category Name | ANDA |
| Labeler Name | Dr. Reddy's Laboratories Ltd |
| 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] |
