Divalproex Sodium
- Product NDC
- 68788-7295
- 11-digit product format
- 687887295
- Labeler code
- 68788
- Product ID
- 68788-7295_ca5c1b13-f3a6-40e3-a3c5-8bce3de56b86
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Divalproex Sodium
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA203730
- Marketing category
- ANDA
- Marketing start
- 2019-01-08
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7295-3 | 68788729503 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7295-3) | 2019-01-08 | 0000-00-00 | No | No | Current |
| 68788-7295-6 | 68788729506 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7295-6) | 2019-01-08 | 0000-00-00 | No | No | Current |
| 68788-7295-9 | 68788729509 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7295-9) | 2019-01-08 | 0000-00-00 | No | No | Current |