Divalproex Sodium
- Product NDC
- 50090-3616
- 11-digit product format
- 500903616
- Labeler code
- 50090
- Product ID
- 50090-3616_7b993d87-1d3a-4dbb-9d3f-08e24a532dc2
- 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
- 2011-04-21
- 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
- 2020-12-31
- 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 |
|---|
| 50090-3616-0 | Divalproex Sodium | 30 in 1 BOTTLE | TABLET, DELAYED RELEASE | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-3616 | DIVALPROEX SODIUM TABLET, DELAYED RELEASE [A-S MEDICATION SOLUTIONS] | 1 | Legacy NDC, 1 package rows | 20190531_d5251aef-7843-427f-8f15-b13117d2eee7.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 |
|---|
| 50090-3616-0 | 50090361600 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-3616-0) | 2018-10-05 | 0000-00-00 | No | No | Current |