NDC 70710-1517-06 - fondaparinux 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
- 70710-1517
- Requested NDC
- 70710-1517-06
- Package NDCs from labels
- 70710-1517-2, 70710-1517-9, 70710-1517-6, 70710-1517-06
- Manufacturer
- Zydus Pharmaceuticals (USA) Inc. | ScinoPharm Taiwan, Ltd.
- Effective date
- 2025-10-28
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| fondaparinux sodium - Zydus Pharmaceuticals (USA) Inc. | ScinoPharm Taiwan, Ltd. | Zydus Pharmaceuticals (USA) Inc. | ScinoPharm Taiwan, Ltd. | 2025-10-28 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70710-1517-2 | fondaparinux sodium | 0.8 mL in 1 SYRINGE | INJECTION, SOLUTION | 0.8 | 20 | |
| 70710-1517-6 | fondaparinux sodium | 10 in 1 CARTON | INJECTION, SOLUTION | 10 | 20 | |
| 70710-1517-9 | fondaparinux sodium | 2 in 1 CARTON | INJECTION, SOLUTION | 2 | 20 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70710-1517 | FONDAPARINUX SODIUM INJECTION, SOLUTION [ZYDUS PHARMACEUTICALS (USA) INC.] | 10 | Current NDC, Legacy NDC, 3 package rows | 20241106_dffbf7c9-495e-4a33-ac76-57b52f014fc2.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 70710-1517-2 | ML - Milliliter | 70710-1517 | 4599a896-57fb-473e-8d3d-1430af82023c | 1 | 2020-02-13 |
| 70710-1517-6 | ML - Milliliter | 70710-1517 | 8790f3ee-c412-446f-b2e2-df0fa17e224a | 1 | 2020-02-13 |
| 70710-1517-9 | ML - Milliliter | 70710-1517 | 480d8d1d-a03f-48f8-a3ce-35af5ebb967f | 1 | 2020-02-13 |
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 |
|---|---|---|---|---|---|---|
| TIS-U-SOL | SODIUM CHLORIDE, POTASSIUM CHLORIDE, MAGNESIUM SULFATE, SODIUM PHOSPHATE, AND POTASSIUM PHOSPHATE | Baxter Healthcare Corporation | 9da4121f-d62d-4da4-8dfb-0494da16015f | 2014-02-21 | 451W47IQ8X | |
| Ringers | SODIUM CHLORIDE, CALCIUM CHLORIDE, POTASSIUM CHLORIDE, | Baxter Healthcare Corporation | e1953d54-818d-46a6-8532-518ebae6d84e | 2012-06-13 | 451W47IQ8X | |
| Lactated Ringers | SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE | Baxter Healthcare Corporation | f09f80bf-2f8b-4420-865d-aec2d5e5cd4d | 2012-06-12 | 451W47IQ8X |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.