Divalproex Sodium
- Product NDC
- 70518-3364
- 11-digit product format
- 705183364
- Labeler code
- 70518
- Product ID
- 70518-3364_d7c436d6-c02f-9e4e-e053-2995a90a2ace
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Divalproex Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA078182
- Marketing category
- ANDA
- Marketing start
- 2022-02-11
- 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 |
|---|
| 70518-3364-0 | 70518336400 | 100 POUCH in 1 BOX (70518-3364-0) > 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-3364-1) | 100 pouch | 2022-02-11 | 0000-00-00 | No | No | Current |