Divalproex Sodium
- Product NDC
- 68071-3553
- 11-digit product format
- 680713553
- Labeler code
- 68071
- Product ID
- 68071-3553_2ad1a6c9-63e3-4ab1-e063-6294a90a552f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Divalproex Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- NuCare 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
- 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 | 1099678 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68071-3553-6 | Divalproex Sodium | 60 in 1 BOTTLE | TABLET, DELAYED RELEASE | 60 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-3553 | DIVALPROEX SODIUM TABLET, DELAYED RELEASE [NUCARE PHARMACEUTICALS,INC.] | 2 | Current NDC, 1 package rows | 20250105_0bef10ed-e4b5-95ae-e063-6294a90a86eb.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 68071-3553-6 | 68071355306 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3553-6) | 2023-12-07 | No | No | Historical |