Divalproex Sodium
- Product NDC
- 10370-510
- 11-digit product format
- 103700510
- Labeler code
- 10370
- Product ID
- 10370-510_a11aa682-1054-4905-84b0-e1b954f3c96b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Divalproex Sodium
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Par Pharmaceutical, Inc.
- Application
- ANDA078445
- Marketing category
- ANDA
- Marketing start
- 2009-02-26
- Marketing end
- 2021-06-30
- Substance
- DIVALPROEX SODIUM
- Active strength
- 250 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 10370-510-50 | 10370051050 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (10370-510-50) | 2009-02-26 | 2021-06-30 | No | No | Current |