Divalproex sodium
- Product NDC
- 72162-2515
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Divalproex sodium
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA202419
- Marketing category
- ANDA
- Substance
- DIVALPROEX SODIUM
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 72162-2515-1 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-2515-1) | 2025-06-09 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Divalproex sodium | Bryant Ranch Prepack | 2025-06-11 | HUMAN PRESCRIPTION DRUG LABEL | 100 |