Divalproex Sodium
- Product NDC
- 68071-4102
- 11-digit product format
- 680714102
- Labeler code
- 68071
- Product ID
- 68071-4102_bb2cb8c2-5ad1-67fb-e053-2a95a90ad1fb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Divalproex Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA079163
- Marketing category
- ANDA
- Marketing start
- 2011-10-01
- Marketing end
- 0000-00-00
- Substance
- DIVALPROEX SODIUM
- Active strength
- 250 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4102-3 | 68071410203 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-4102-3) | 2017-09-27 | 0000-00-00 | No | No | Current |
| 68071-4102-5 | 68071410205 | 45 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-4102-5) | 2017-09-27 | 0000-00-00 | No | No | Current |
| 68071-4102-6 | 68071410206 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-4102-6) | 2017-09-27 | 0000-00-00 | No | No | Current |