Divalproex Sodium
- Product NDC
- 50090-4409
- 11-digit product format
- 500904409
- Labeler code
- 50090
- Product ID
- 50090-4409_c8aa2974-172f-465b-b6d2-6253c5add57d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Divalproex Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA079163
- Marketing category
- ANDA
- Marketing start
- 2011-10-01
- 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
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 |
|---|
| 50090-4409-0 | 50090440900 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-4409-0) | 2019-07-15 | 0000-00-00 | No | No | Current |