NDC 55111-533-79 - Divalproex Sodium
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 55111-533
- Requested NDC
- 55111-533-79
- Package NDCs from labels
- 55111-533-30, 55111-533-60, 55111-533-01, 55111-533-05, 55111-533-79, 55111-533-78
- Manufacturer
- NCS HealthCare of KY, LLC dba Vangard Labs
- Effective date
- 2026-09-18
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Divalproex Sodium - NCS HealthCare of KY, LLC dba Vangard Labs | NCS HealthCare of KY, LLC dba Vangard Labs | 2026-09-18 | HUMAN PRESCRIPTION DRUG LABEL |
| Divalproex Sodium - Major Pharmaceuticals | Major Pharmaceuticals | 2026-07-23 | HUMAN PRESCRIPTION DRUG LABEL |
| Divalproex Sodium - Dr. Reddy's Laboratories Ltd | Dr. Reddy's Laboratories Limite - FTO 3 | Dr. Reddy's Laboratories Ltd | Dr. Reddy's Laboratories Limite - FTO 3 | 2026-07-07 | HUMAN PRESCRIPTION DRUG LABEL |
| Divalproex Sodium - REMEDYREPACK INC. | REMEDYREPACK INC. | 2026-07-02 | HUMAN PRESCRIPTION DRUG LABEL |
| Divalproex Sodium - Coupler LLC | Coupler LLC | 2026-06-01 | HUMAN PRESCRIPTION DRUG LABEL |
| Divalproex Sodium - REMEDYREPACK INC. | REMEDYREPACK INC. | 2022-06-10 | HUMAN PRESCRIPTION DRUG LABEL |
| Divalproex Sodium - Safecor Health, LLC | Safecor Health, LLC | 2022-01-26 | HUMAN PRESCRIPTION DRUG LABEL |
| Divalproex Sodium - A-S Medication Solutions | A-S Medication Solutions | 2018-08-07 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 55111-533-01 | Divalproex Sodium | 100 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 100 | 27 | |
| 55111-533-05 | Divalproex Sodium | 500 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 500 | 27 | |
| 55111-533-30 | Divalproex Sodium | 30 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 30 | 27 | |
| 55111-533-60 | Divalproex Sodium | 60 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 60 | 27 | |
| 55111-533-78 | Divalproex Sodium | 10 in 1 CARTON | TABLET, EXTENDED RELEASE | 10 | 27 | |
| 55111-533-79 | Divalproex Sodium | 10 in 1 BLISTER PACK | TABLET, EXTENDED RELEASE | 10 | 27 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 55111-533-01 | EA - Each | 55111-533 | c478261d-9125-44ed-a3a2-b737d3373d93 | 1 | 2013-09-04 |
| 55111-533-05 | EA - Each | 55111-533 | d4335507-dcdd-4e0d-bb88-c4efff7d82e6 | 1 | 2013-09-04 |
DailyMed Socrata Ingredients#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.