NDC 64725-0314
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 Tya Pharmaceuticals. The primary component is Divalproex Sodium.
Product ID | 64725-0314_af3febff-f6b0-4bb3-9f83-142ef96135e9 |
NDC | 64725-0314 |
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 | 2000-08-04 |
Marketing Category | NDA AUTHORIZED GENERIC / NDA AUTHORIZED GENERIC |
Application Number | NDA021168 |
Labeler Name | TYA Pharmaceuticals |
Substance Name | DIVALPROEX SODIUM |
Active Ingredient Strength | 250 mg/1 |
Pharm Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC] |
NDC Exclude Flag | E |
Listing Certified Through | 2017-12-31 |