Drug application
METHYLPHENIDATE (METHYLPHENIDATE)
Drugs@FDA ANDA 206497 · MYLAN TECH VIATRIS
Key facts
| Drug name | METHYLPHENIDATE |
|---|---|
| Active ingredients | METHYLPHENIDATE |
| Application type | ANDA |
| Application number | 206497 |
| Company | MYLAN TECH VIATRIS |
| Dosage forms | FILM, EXTENDED RELEASE, TRANSDERMAL |
| Strength | 10MG/9HR (1.1MG/HR) |
| Marketing status | Prescription |
| TE codes | AB |
| Reference listed drug | No |
| Latest submission status date | Mar 14, 2022 |
At a glance
- 1–9 Submissions
- 1–9 Supplements
- None Label versions
- 1–9 Products
- 1–9 Therapeutic equivalents
- Yes FDA letters on file
- Yes FDA reviews on file
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About Drugs@FDA applications
Drugs@FDA covers FDA-approved brand-name and generic drugs and therapeutic biologics, with their applications (NDA, ANDA or BLA), products, submissions and labels.
Source: U.S. Food and Drug Administration (FDA), Drugs@FDA · Source date: