FDA NDC Directory · JSON-LD · Markdown
NDC 50242-260 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION
| Generic name | pertuzumab, trastuzumab, and hyaluronidase-zzxf |
|---|---|
| Labeler / Manufacturer | Genentech, Inc. |
| Marketing category | Biologic License Application · App BLA761170 |
| Dosage form / route | INJECTION, SOLUTION · SUBCUTANEOUS |
| Active ingredients | HYALURONIDASE (HUMAN RECOMBINANT) (20000 U/10mL) PERTUZUMAB (600 mg/10mL) TRASTUZUMAB (600 mg/10mL) |
| Marketing started | 20200629 |
| Package count | 2 |
Source: openFDA. Public-domain (CC0).