Divalproex sodium
- Product NDC
- 50090-5783
- 11-digit product format
- 500905783
- Labeler code
- 50090
- Product ID
- 50090-5783_2d888afa-bc4d-463e-8d3f-88743a09965f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Divalproex sodium
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA209286
- Marketing category
- ANDA
- Marketing start
- 2020-09-18
- Marketing end
- 0000-00-00
- Substance
- DIVALPROEX SODIUM
- Active strength
- 500 1/1
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5783-0 | 50090578300 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5783-0) | 2021-10-08 | 0000-00-00 | No | No | Current |
| 50090-5783-1 | 50090578301 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5783-1) | 2021-10-08 | 0000-00-00 | No | No | Current |