Divalproex Sodium
- Product NDC
- 68788-8145
- 11-digit product format
- 687888145
- Labeler code
- 68788
- Product ID
- 68788-8145_cba2c4b2-7c5c-4e74-9217-693e69bb3e07
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Divalproex Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA090554
- Marketing category
- ANDA
- Marketing start
- 2022-02-22
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 644VL95AO6 | DIVALPROEX SODIUM | 76584-70-8 | DIVALPROEX SODIUM |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-8145-3 | 68788814503 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8145-3) | 2022-02-22 | 0000-00-00 | No | No | Current |