NDC 73309-217 - Actinomycin D (Dactinomycin)
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
- 73309-217
- Package NDCs from labels
- 73309-217-01
- Manufacturer
- BLUEBAY SHANDONG CO.,LTD
- Effective date
- 2020-12-31
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Actinomycin D (Dactinomycin) - BLUEBAY SHANDONG CO.,LTD | BLUEBAY SHANDONG CO.,LTD | 2020-12-31 | BULK INGREDIENT |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 73309-217-01 | Actinomycin D (Dactinomycin) | 1 g in 1 VIAL | POWDER | 1 | 1 |
DailyMed Dashboard NDC Coverage#
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 |
|---|---|---|---|---|---|---|
| DACTINOMYCIN | DACTINOMYCIN | Eugia US LLC | 5da55538-2602-4704-a9da-603c9f7ff7dc | 2024-06-18 | Warnings, Adverse reactions | 1CC1JFE158 |
| dactinomycin | DACTINOMYCIN | XGen Pharmaceuticals DJB, Inc. | efe03d73-eb11-45ff-a3cb-09a540ed352f | 2024-05-28 | Warnings, Adverse reactions | 1CC1JFE158 |
| Dactinomycin | DACTINOMYCIN | Hisun Pharmaceuticals USA, Inc. | 95d5c152-aa00-41e6-83e8-8df374a56447 | 2024-05-08 | Warnings, Adverse reactions | 1CC1JFE158 |
| DACTINOMYCIN | DACTINOMYCIN | Eugia US LLC | aa047ee8-f2e8-4720-84b1-d1c4532d6c63 | 2023-12-20 | Warnings, Adverse reactions | 1CC1JFE158 |
| Dactinomycin | DACTINOMYCIN | Meitheal Pharmaceuticals Inc. | 2aaca42a-3b79-4151-a727-83253556a540 | 2020-11-13 | Warnings, Adverse reactions | 1CC1JFE158 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.