NDC 53808-1061
Divalproex Sodium Extended-Release
Divalproex Sodium
Divalproex Sodium Extended-Release is a Oral Tablet, Extended Release in the Human Prescription Drug category. It is labeled and distributed by State Of Florida Doh Central Pharmacy. The primary component is Divalproex Sodium.
| Product ID | 53808-1061_77f11b3f-cb30-432a-aa27-9c9286c91da2 |
| NDC | 53808-1061 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Divalproex Sodium Extended-Release |
| Generic Name | Divalproex Sodium |
| Dosage Form | Tablet, Extended Release |
| Route of Administration | ORAL |
| Marketing Start Date | 2014-11-01 |
| Marketing Category | NDA AUTHORIZED GENERIC / NDA AUTHORIZED GENERIC |
| Application Number | NDA021168 |
| Labeler Name | State of Florida DOH Central Pharmacy |
| Substance Name | DIVALPROEX SODIUM |
| Active Ingredient Strength | 500 mg/1 |
| Pharm Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2019-12-31 |