Divalproex Sodium
- Product NDC
- 72789-353
- 11-digit product format
- 727890353
- Labeler code
- 72789
- Product ID
- 72789-353_4bbf5334-b723-117e-e063-6394a90a5888
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Divalproex Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA078597
- Marketing category
- ANDA
- Marketing start
- 2008-07-29
- 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
- 2027-12-31
- 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 |
|---|
| 72789-353-01 | 72789035301 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-353-01) | 2023-10-18 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Divalproex Sodium | PD-Rx Pharmaceuticals, Inc. | 2026-02-26 | HUMAN PRESCRIPTION DRUG LABEL | 32 |