Divalproex Sodium
- Product NDC
- 68001-105
- 11-digit product format
- 680010105
- Labeler code
- 68001
- Product ID
- 68001-105_304dd980-5e9b-d776-e063-6394a90aa9cf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Divalproex Sodium
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- BluePoint Laboratories
- Application
- ANDA078239
- Marketing category
- ANDA
- Marketing start
- 2013-10-08
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Divalproex Sodium
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DIVALPROEX SODIUM | 250 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 644VL95AO6 |
| Rxcui | 1099563, 1099569 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68001-105-00 | Divalproex Sodium | 100 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 100 | | 30 |
| 68001-105-03 | Divalproex Sodium | 500 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 500 | | 30 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68001-105 | DIVALPROEX SODIUM TABLET, FILM COATED, EXTENDED RELEASE [BLUEPOINT LABORATORIES] | 30 | Current NDC, Legacy NDC, 2 package rows | 20250316_1b12c694-e120-45f6-ad28-36373e2c5378.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68001-105-00 | 68001010500 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-105-00) | 2013-10-08 | 0000-00-00 | No | No | Current |
| 68001-105-03 | 68001010503 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-105-03) | 2013-10-08 | 0000-00-00 | No | No | Current |