Divalproex Sodium
- Product NDC
- 50090-5843
- 11-digit product format
- 500905843
- Labeler code
- 50090
- Product ID
- 50090-5843_8e66699d-7131-4b84-9371-52d72dc39125
- 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
- Marketing start
- 2014-10-24
- Marketing end
- 0000-00-00
- Substance
- DIVALPROEX SODIUM
- Active strength
- 500 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5843-0 | 50090584300 | 33 BLISTER PACK in 1 BOX, UNIT-DOSE (50090-5843-0) > 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK | 33 blister pack | 2021-11-03 | 0000-00-00 | No | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Divalproex Sodium | A-S Medication Solutions | 2021-11-08 | Human Prescription Drug Label | 1 |