Divalproex sodium
- Product NDC
- 0615-1393
- 11-digit product format
- 006151393
- Labeler code
- 0615
- Product ID
- 0615-1393_0db335ac-0715-4471-a2e2-6d317d30ed5a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Divalproex sodium
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA078979
- Marketing category
- ANDA
- Marketing start
- 2009-01-23
- Marketing end
- 2020-08-31
- Substance
- DIVALPROEX SODIUM
- Active strength
- 125 mg/1
- Pharmacologic classes
- Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record