NDC 73309-001 - Chlorambucil
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
- 73309-001
- Package NDCs from labels
- 73309-001-02, 73309-001-03, 73309-001-04, 73309-001-01
- Manufacturer
- BLUEBAY SHANDONG CO.,LTD
- Effective date
- 2020-04-16
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Chlorambucil - BLUEBAY SHANDONG CO.,LTD | BLUEBAY SHANDONG CO.,LTD | 2020-04-16 | BULK INGREDIENT |
| Chlorambucil - BLUEBAY SHANDONG CO.,LTD | BLUEBAY SHANDONG CO.,LTD | 2019-08-21 | BULK INGREDIENT |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 73309-001-02 | Chlorambucil | 100 g in 1 JAR | POWDER | 100 | 2 | |
| 73309-001-03 | Chlorambucil | 500 g in 1 JAR | POWDER | 500 | 2 | |
| 73309-001-04 | Chlorambucil | 10 g in 1 JAR | POWDER | 10 | 2 | |
| 73309-001-01 | Chlorambucil | 250 g in 1 JAR | POWDER | 250 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 73309-001 | CHLORAMBUCIL POWDER [BLUEBAY SHANDONG CO.,LTD] | 2 | 3 package rows | 20200417_b785e9eb-c1b5-46eb-9a08-294f65d0e168.zip |
| 73309-001 | CHLORAMBUCIL POWDER [BLUEBAY SHANDONG CO.,LTD] | 1 | 1 package rows | 20190822_c524b8db-0954-48e3-b8dd-8ed4705d6d94.zip |
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 |
|---|---|---|---|---|---|---|
| LEUKERAN | CHLORAMBUCIL | Waylis Therapeutics LLC | 58a3c995-5ad6-465d-8437-5970c9088213 | 2025-01-08 | Boxed warning, Warnings, Adverse reactions | 18D0SL7309 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.