Divalproex Sodium
- Product NDC
- 0615-8242
- 11-digit product format
- 006158242
- Labeler code
- 0615
- Product ID
- 0615-8242_ba206eb8-9de1-4525-b437-dda33c89c7aa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- divalproex sodium
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA077567
- Marketing category
- ANDA
- Marketing start
- 2009-01-29
- Marketing end
- 2021-09-30
- 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 |
|---|
| 0615-8242-39 | 00615824239 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0615-8242-39) | 2018-11-01 | 2021-09-30 | No | No | Current |