NDC 24839-333 - CARDIOTEK-RX
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
- 24839-333
- Package NDCs from labels
- 24839-333-30, 24839-333-99
- Manufacturer
- SJ PHARMACEUTICALS, LLC | NEXGEN PHARMA
- Effective date
- 2018-04-26
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| CARDIOTEK-RX - SJ PHARMACEUTICALS, LLC | NEXGEN PHARMA | SJ PHARMACEUTICALS, LLC | NEXGEN PHARMA | 2018-04-26 | DIETARY SUPPLEMENT |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 24839-333-30 | CARDIOTEK-RX | 1740 mg in 1 BOTTLE | TABLET, COATED | 1740 | 1 | |
| 24839-333-99 | CARDIOTEK-RX | 58 mg in 1 DOSE PACK | TABLET, COATED | 58 | 1 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 24839-333-30 | EA - Each | 24839-333 | a04211c9-00f7-41fd-a302-9393c08b12f4 | 1 | 2018-05-09 |
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.
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.