Divalproex Sodium
- Product NDC
- 55700-939
- 11-digit product format
- 557000939
- Labeler code
- 55700
- Product ID
- 55700-939_a00d2ac8-384f-4140-a9ab-02cc011982bb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Divalproex Sodium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Quality Care Products, LLC
- Application
- ANDA079163
- Marketing category
- ANDA
- Marketing start
- 2021-09-10
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55700-939 | DIVALPROEX SODIUM TABLET, DELAYED RELEASE [QUALITY CARE PRODUCTS, LLC] | 4 | Legacy NDC | 20241220_8fff0e14-fd53-47d6-b4e7-22880e5aae12.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-939-60 | 55700093960 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (55700-939-60) | 2021-09-10 | 0000-00-00 | No | No | Current |