DIVALPROEX SODIUM
- Product NDC
- 61919-648
- 11-digit product format
- 619190648
- Labeler code
- 61919
- Product ID
- 61919-648_9c93c4a2-a592-5060-e053-2a95a90afd72
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DIVALPROEX SODIUM
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA078597
- Marketing category
- ANDA
- Marketing start
- 2014-01-01
- 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
- 2021-12-31
- 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 |
|---|
| 61919-648-30 | DIVALPROEX SODIUM | 30 in 1 BOTTLE | TABLET, DELAYED RELEASE | 30 | | 3 |
| 61919-648-60 | DIVALPROEX SODIUM | 60 in 1 BOTTLE | TABLET, DELAYED RELEASE | 60 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-648 | DIVALPROEX SODIUM TABLET, DELAYED RELEASE [DIRECT RX] | 3 | Legacy NDC, 2 package rows | 20200121_918237c3-3a3e-4ec0-9479-7fd727caf1e5.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 |
|---|
| 61919-648-30 | 61919064830 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (61919-648-30) | 2014-01-01 | 0000-00-00 | No | No | Current |
| 61919-648-60 | 61919064860 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (61919-648-60) | 2014-01-01 | 0000-00-00 | No | No | Current |