FDA approval · Drugs@FDA
OPDIVO QVANTIGnivolumab, hyaluronidase-nvhy
BLA761429 ·
FDA approved the original biologics license application for OPDIVO QVANTIG on December 27, 2024, sponsored by BRISTOL-MYERS SQUIBB. FDA’s record shows no approved efficacy supplement on the application since.
- Application
- BLA761429
- Sponsor
- BRISTOL-MYERS SQUIBB
- Original approval
- Review
- standard review
- Submission class
- Type 9 - New indication submitted as distinct BLA, consolidated
- Active ingredient
- nivolumab, hyaluronidase-nvhy
Browse every approval whose brand starts with O, or the complete response letters FDA has published — the applications it did not approve.
Products under this application
| Ingredient and strength | Form | Route | Marketing status |
|---|---|---|---|
| nivolumab 600MG; hyaluronidase-nvhy 10000 UNITS PER 5ML(120MG/2000UNITS PER ML) | INJECTABLE | INJECTION | Prescription |
Approved efficacy supplements
An efficacy supplement is how a sponsor asks FDA to approve a change that needs clinical evidence — most often a new indication. FDA’s record gives each one a submission number, a date and a review priority. It does not say what any supplement approved, so neither does this page. The approval letter and label for each are on accessdata.fda.gov under the application number.
FDA’s record shows no approved efficacy supplement on this application.
Source: FDA’s Drugs@FDA application file, via openFDA (export 2026-09-03). Every field on this page comes from that record.
Other approvals to BRISTOL-MYERS SQUIBB
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