FDA approved the original new drug application for ULTIVA on July 12, 1996, sponsored by MYLAN INSTITUTIONAL. FDA classed that submission a new molecular entity, which makes it the first approval of remifentanil hydrochloride in any product. FDA has approved 3 efficacy supplements on the application since, the most recent on March 8, 2004.
- Application
- NDA020630
- Sponsor
- MYLAN INSTITUTIONAL
- Original approval
- Review
- standard review
- Submission class
- Type 1 - New Molecular Entity
- Active ingredient
- remifentanil hydrochloride
Browse every approval whose brand starts with U, 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 |
|---|---|---|---|
| remifentanil hydrochloride EQ 5MG BASE/VIAL | INJECTABLE | INJECTION | Prescription |
| remifentanil hydrochloride EQ 1MG BASE/VIAL | INJECTABLE | INJECTION | Prescription |
| remifentanil hydrochloride EQ 2MG BASE/VIAL | 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.
| Approved | Supplement | Review |
|---|---|---|
| S-1 | standard | |
| S-2 | standard | |
| S-5 | standard |
FDA records other approved supplements on this application, by the class code it assigns them: Labeling 7 · Manufacturing (CMC) 6. Those are changes to the label or to how the drug is made rather than new clinical evidence, so they are counted here and not listed.
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 MYLAN INSTITUTIONAL
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