NDC 70518-1769-2 - Carbamazepine
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
- 70518-1769
- Requested NDC
- 70518-1769-2
- Package NDCs from labels
- 70518-1769-0, 70518-1769-2, 70518-1769-1
- Manufacturer
- REMEDYREPACK INC.
- Effective date
- 2023-03-06
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Carbamazepine - REMEDYREPACK INC. | REMEDYREPACK INC. | 2023-03-06 | HUMAN PRESCRIPTION DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| CARBAMAZEPINE | CARBAMAZEPINE | Proficient Rx LP | bf61798e-c07e-4959-909a-2b4c2c83b532 | 2019-10-01 | Boxed warning, Warnings, Adverse reactions | 33CM23913M |
| CARBAMAZEPINE | CARBAMAZEPINE | Aphena Pharma Solutions - Tennessee, LLC | c1fc31ef-6b2e-4de4-a185-ec44e94e7b40 | 2016-06-02 | Boxed warning, Warnings, Adverse reactions | 33CM23913M |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.