Divalproex Sodium
- Product NDC
- 50090-5843
- 11-digit product format
- 500905843
- Labeler code
- 50090
- Product ID
- 50090-5843_8e66699d-7131-4b84-9371-52d72dc39125
- 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
- 2014-10-24
- 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
- 2022-12-31
- 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 |
|---|
| 50090-5843-0 | Divalproex Sodium | 1 in 1 BLISTER PACK | TABLET, DELAYED RELEASE | 1 | | 1 |
| 50090-5843-0 | Divalproex Sodium | 33 in 1 BOX, UNIT-DOSE | TABLET, DELAYED RELEASE | 33 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-5843 | DIVALPROEX SODIUM TABLET, DELAYED RELEASE [A-S MEDICATION SOLUTIONS] | 1 | Legacy NDC, 2 package rows | 20211109_f3a92756-72ad-4429-9c7a-b38de0695d3d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5843-0 | 50090584300 | 33 BLISTER PACK in 1 BOX, UNIT-DOSE (50090-5843-0) > 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK | 33 blister pack | 2021-11-03 | 0000-00-00 | No | No | Current |