Divalproex Sodium
- Product NDC
- 55154-7640
- 11-digit product format
- 551547640
- Labeler code
- 55154
- Product ID
- 55154-7640_f6cd31ed-db2b-4e11-80a7-d2e835c00f05
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Divalproex Sodium
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Cardinal Health 107, LLC
- Application
- ANDA090070
- Marketing category
- ANDA
- Marketing start
- 2013-08-11
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55154-7640-0 | 55154764000 | 10 BLISTER PACK in 1 BAG (55154-7640-0) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 10 blister pack | 2013-08-11 | 0000-00-00 | No | No | Current |