Divalproex Sodium
- Product NDC
- 33261-641
- 11-digit product format
- 332610641
- Labeler code
- 33261
- Product ID
- 33261-641_c587a83e-6bd2-4645-8044-0884fbb2bc4f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Divalproex Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Aidarex Pharmaceuticals LLC
- Application
- ANDA078597
- Marketing category
- ANDA
- Marketing start
- 2008-07-29
- Marketing end
- 0000-00-00
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 33261-641-30 | Divalproex Sodium | 30 in 1 BOTTLE, PLASTIC | TABLET, DELAYED RELEASE | 30 | | 1 |
| 33261-641-60 | Divalproex Sodium | 60 in 1 BOTTLE, PLASTIC | TABLET, DELAYED RELEASE | 60 | | 1 |
| 33261-641-90 | Divalproex Sodium | 90 in 1 BOTTLE, PLASTIC | TABLET, DELAYED RELEASE | 90 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 33261-641 | DIVALPROEX SODIUM TABLET, DELAYED RELEASE [AIDAREX PHARMACEUTICALS LLC] | 1 | Legacy NDC, 3 package rows | 20140106_51132e43-6fda-4cd4-a818-cfd399264e89.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 33261-641-30 | 33261064130 | 30 in 1 BOTTLE, PLASTIC | Historical |
| 33261-641-60 | 33261064160 | 60 in 1 BOTTLE, PLASTIC | Historical |
| 33261-641-90 | 33261064190 | 90 in 1 BOTTLE, PLASTIC | Historical |