NDC 10139-319 - Melphalan Hydrochloride
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
- 10139-319
- Package NDCs from labels
- 10139-319-10
- Manufacturer
- GeneraMedix Inc. | Coldstream Laboratories Inc
- Effective date
- 2009-10-27
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Melphalan Hydrochloride - GeneraMedix Inc. | Coldstream Laboratories Inc | GeneraMedix Inc. | Coldstream Laboratories Inc | 2009-10-27 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 10139-319-10 | Melphalan Hydrochloride | 10 mL in 1 VIAL, SINGLE-DOSE | INJECTION, POWDER, FOR SOLUTION | 10 mL | 50 mg in 10mL | 2 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| MELPHALAN HYDROCHLORIDE | ACTIVE INGREDIENT | 1VXP4V453T | MELPHALAN HYDROCHLORIDE KIT [GENERAMEDIX INC.] | 2 | |
| MELPHALAN | ACTIVE MOIETY | Q41OR9510P | MELPHALAN HYDROCHLORIDE KIT [GENERAMEDIX INC.] | 2 | |
| POVIDONE | INACTIVE INGREDIENT | FZ989GH94E | MELPHALAN HYDROCHLORIDE KIT [GENERAMEDIX INC.] | 2 |
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.