Divalproex Sodium
- Product NDC
- 71335-2862
- 11-digit product format
- 713352862
- Labeler code
- 71335
- Product ID
- 71335-2862_41d88ff2-2260-8447-e063-6294a90aea0e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Divalproex Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA079163
- Marketing category
- ANDA
- Marketing start
- 2011-10-01
- 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 |
|---|
| 71335-2862-1 | 71335286201 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2862-1) | 2025-10-23 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Divalproex Sodium | Bryant Ranch Prepack | 2025-10-23 | HUMAN PRESCRIPTION DRUG LABEL | 100 |