divalproex sodium
- Product NDC
- 82804-233
- 11-digit product format
- 828040233
- Labeler code
- 82804
- Product ID
- 82804-233_15ffe3d8-d483-4c45-adc4-1cc8a5b68d19
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- divalproex sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA078853
- Marketing category
- ANDA
- Marketing start
- 2024-06-26
- 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
- 2026-12-31
- Current FDA listing
- Yes
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 | Sample | Exclude flag | Status |
|---|
| 82804-233-30 | 82804023330 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (82804-233-30) | 2025-08-06 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| divalproex sodium | Proficient Rx LP | 2025-08-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |