Divalproex Sodium
- Product NDC
- 70518-2510
- 11-digit product format
- 705182510
- Labeler code
- 70518
- Product ID
- 70518-2510_b9fc93b9-b5ff-5cd9-e053-2995a90a68e3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Divalproex Sodium
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA203730
- Marketing category
- ANDA
- Marketing start
- 2019-12-27
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2510-0 | 70518251000 | 100 POUCH in 1 BOX (70518-2510-0) > 1 TABLET, EXTENDED RELEASE in 1 POUCH (70518-2510-1) | 100 pouch | 2019-12-27 | 0000-00-00 | No | No | Current |
| 70518-2510-2 | 70518251002 | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-2510-2) | | 2020-03-09 | 0000-00-00 | No | No | Current |
| 70518-2510-3 | 70518251003 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2510-3) | | 2020-09-04 | 0000-00-00 | No | No | Current |
| 70518-2510-4 | 70518251004 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2510-4) | | 2020-09-30 | 0000-00-00 | No | No | Current |