Divalproex Sodium
- Product NDC
- 70518-0613
- 11-digit product format
- 705180613
- Labeler code
- 70518
- Product ID
- 70518-0613_a55f5b00-16cb-3c98-e053-2a95a90a82dc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Divalproex Sodium
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA090070
- Marketing category
- ANDA
- Marketing start
- 2017-07-12
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record