Divalproex Sodium
- Product NDC
- 50090-7121
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Divalproex Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA090554
- Marketing category
- ANDA
- Substance
- DIVALPROEX SODIUM
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 50090-7121-0 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7121-0) | 2024-03-27 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Divalproex Sodium | A-S Medication Solutions | 2024-04-02 | Human Prescription Drug Label | 1 |