Divalproex Sodium
- Product NDC
- 60687-211
- 11-digit product format
- 606870211
- Labeler code
- 60687
- Product ID
- 60687-211_ea3f737d-0c25-5b4c-e053-2995a90a7682
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Divalproex Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA090554
- Marketing category
- ANDA
- Marketing start
- 2016-09-02
- 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 Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60687-211 | DIVALPROEX SODIUM TABLET, DELAYED RELEASE [AMERICAN HEALTH PACKAGING] | 16 | Legacy NDC | 20250216_23dd3ef2-3ece-49ae-9133-f0ce10fd68fc.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60687-211-21 | 60687021121 | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-211-21) > 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-211-11) | 30 blister pack | 2016-09-02 | 0000-00-00 | No | No | Current |