Divalproex Sodium
- Product NDC
- 0615-8329
- 11-digit product format
- 006158329
- Labeler code
- 0615
- Product ID
- 0615-8329_acb4c5c5-9b7a-4a38-a290-9f40817da462
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Divalproex Sodium
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA090161
- Marketing category
- ANDA
- Marketing start
- 2013-08-11
- Marketing end
- 2022-05-31
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0615-8329-39 | 00615832939 | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-8329-39) | 2020-01-07 | 2022-05-31 | No | No | Current |