FDA NDC Directory · JSON-LD · Markdown
NDC 25682-016 · HUMAN PRESCRIPTION DRUG · SOLUTION
| Generic name | ASFOTASE ALFA |
|---|---|
| Labeler / Manufacturer | Alexion Pharmaceuticals, Inc. |
| Marketing category | Biologic License Application · App BLA125513 |
| Dosage form / route | SOLUTION · SUBCUTANEOUS |
| Active ingredients | ASFOTASE ALFA (40 mg/mL) |
| Marketing started | 20151023 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).