NDC 52609-3003 - ALKERAN
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
- 52609-3003
- Package NDCs from labels
- 52609-3003-0
- Manufacturer
- ApoPharma USA, Inc.
- Effective date
- 2022-12-05
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| ALKERAN ® (melphalan hydrochloride) for Injection | ApoPharma USA, Inc. | 2022-12-05 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| MELPHALAN HYDROCHLORIDE | ACTIVE INGREDIENT | 1VXP4V453T | ALKERAN (MELPHALAN HYDROCHLORIDE) KIT [APO-PHARMA USA, INC] | 6 | |
| MELPHALAN | ACTIVE MOIETY | Q41OR9510P | ALKERAN (MELPHALAN HYDROCHLORIDE) KIT [APO-PHARMA USA, INC] | 6 | |
| POVIDONES | INACTIVE INGREDIENT | FZ989GH94E | ALKERAN (MELPHALAN HYDROCHLORIDE) KIT [APO-PHARMA USA, INC] | 6 |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.