0615-8377Level 3
Divalproex sodium (Divalproex sodium)
**Product type:** Human Prescription Drug
**Active ingredient:** DIVALPROEX SODIUM
**Strength:** 500 mg/1
**Dosage form:** Tablet, Extended Release
**Route:** Oral
**Labeler:** NCS HealthCare of KY, LLC dba Vangard Labs
**Marketing category:** ANDA (ANDA209286)
**Pharmacologic class:** Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE], Mood Stabilizer [EPC]
GET
/api/v1/systems/ndc_fda/nodes/0615-8377Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.