Divalproex Sodium
- Product NDC
- 50090-5842
- 11-digit product format
- 500905842
- Labeler code
- 50090
- Product ID
- 50090-5842_3a685c59-b8b7-49ad-b952-572fa0acfca8
- 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
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 |
|---|
| 50090-5842-0 | 50090584200 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5842-0) | 2021-11-03 | 0000-00-00 | No | No | Current |