FDA approval · Drugs@FDA
DYANAVEL XR 20amphetamine, amphetamine aspartate/dextroamphetamine sulfate
NDA210526 ·
FDA approved the original new drug application for DYANAVEL XR 20 on November 4, 2021, sponsored by TRIS PHARMA INC. FDA’s record shows no approved efficacy supplement on the application since.
- Application
- NDA210526
- Sponsor
- TRIS PHARMA INC
- Original approval
- Review
- standard review
- Submission class
- Type 3 - New Dosage Form
- Active ingredient
- amphetamine, amphetamine aspartate/dextroamphetamine sulfate
Browse every approval whose brand starts with D, 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 |
|---|---|---|---|
| amphetamine 16MG; amphetamine aspartate/dextroamphetamine sulfate EQ 4MG BASE | TABLET, EXTENDED RELEASE | ORAL | Prescription |
| amphetamine 8MG; amphetamine aspartate/dextroamphetamine sulfate EQ 2MG BASE | TABLET, EXTENDED RELEASE | ORAL | Prescription |
| amphetamine 12MG; amphetamine aspartate/dextroamphetamine sulfate EQ 3MG BASE | TABLET, EXTENDED RELEASE | ORAL | Prescription |
| amphetamine 4MG; amphetamine aspartate/dextroamphetamine sulfate EQ 1MG BASE | TABLET, EXTENDED RELEASE | ORAL | 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.
FDA records other approved supplements on this application, by the class code it assigns them: Labeling 5. 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 TRIS PHARMA INC
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