divalproex sodium
- Product NDC
- 50268-258
- 11-digit product format
- 502680258
- Labeler code
- 50268
- Product ID
- 50268-258_d5cef1ed-0256-438c-e053-2a95a90a77a6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- divalproex sodium
- Dosage form
- CAPSULE, COATED PELLETS
- Route
- ORAL
- Labeler
- AvPAK
- Application
- ANDA078919
- Marketing category
- ANDA
- Marketing start
- 2016-07-14
- Marketing end
- 0000-00-00
- Substance
- DIVALPROEX SODIUM
- Active strength
- 125 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 |
|---|
| 50268-258-13 | 50268025813 | 30 BLISTER PACK in 1 BOX (50268-258-13) > 1 CAPSULE, COATED PELLETS in 1 BLISTER PACK (50268-258-11) | 30 blister pack | 2016-07-14 | 0000-00-00 | No | No | Current |