FDA NDC Directory · JSON-LD · Markdown
NDC 50242-245 · 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) (30000 U/15mL) PERTUZUMAB (1200 mg/15mL) TRASTUZUMAB (600 mg/15mL) |
| Marketing started | 20200629 |
| Package count | 2 |
Source: openFDA. Public-domain (CC0).