Drug application
METHYLPHENIDATE HYDROCHLORIDE (METHYLPHENIDATE HYDROCHLORIDE)
Drugs@FDA ANDA 206726 · AUROLIFE PHARMA LLC
Key facts
| Drug name | METHYLPHENIDATE HYDROCHLORIDE |
|---|---|
| Active ingredients | METHYLPHENIDATE HYDROCHLORIDE |
| Application type | ANDA |
| Application number | 206726 |
| Company | AUROLIFE PHARMA LLC |
| Dosage forms | TABLET, EXTENDED RELEASE, ORAL |
| Strength | 18MG |
| Marketing status | Prescription |
| TE codes | AB |
| Reference listed drug | No |
| Latest submission status date | Oct 21, 2016 |
At a glance
- 1–9 Submissions
- 1–9 Supplements
- None Label versions
- 1–9 Products
- 10–99 Therapeutic equivalents
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.