Divalproex Sodium
- Product NDC
- 70518-2665
- 11-digit product format
- 705182665
- Labeler code
- 70518
- Product ID
- 70518-2665_ec940c08-52e9-5812-e053-2995a90a932c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Divalproex Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA078597
- Marketing category
- ANDA
- Marketing start
- 2020-03-30
- 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
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-2665 | DIVALPROEX SODIUM TABLET, DELAYED RELEASE [REMEDYREPACK INC.] | 11 | Legacy NDC | 20250327_fcdd28a5-6199-4da2-8342-8bfc89e6c48b.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2665-0 | 70518266500 | 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-2665-0) | 2020-03-30 | 0000-00-00 | No | No | Current |