Divalproex Sodium
- Product NDC
- 50090-3872
- 11-digit product format
- 500903872
- Labeler code
- 50090
- Product ID
- 50090-3872_7787a251-8971-45c8-bbab-b0e6bf8bf3d9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Divalproex Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA079163
- Marketing category
- ANDA
- Marketing start
- 2011-10-01
- Marketing end
- 0000-00-00
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record