Divalproex Sodium
- Product NDC
- 0093-7439
- 11-digit product format
- 000937439
- Labeler code
- 0093
- Product ID
- 0093-7439_e67f291f-cfd5-4c7e-8f6a-e961f720996f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Divalproex Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Application
- ANDA076941
- Marketing category
- ANDA
- Marketing start
- 2008-07-29
- Marketing end
- 2019-04-30
- 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