Divalproex Sodium
- Product NDC
- 0615-7555
- 11-digit product format
- 006157555
- Labeler code
- 0615
- Product ID
- 0615-7555_5d008b40-c3a8-48e1-8b9a-142590e1a287
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- divalproex sodium
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA077567
- Marketing category
- ANDA
- Marketing start
- 2002-02-28
- Marketing end
- 2020-08-31
- Substance
- DIVALPROEX SODIUM
- Active strength
- 500 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