Drug application
DOXYCYCLINE HYCLATE (DOXYCYCLINE HYCLATE)
Drugs@FDA ANDA 208741 · LUPIN
Key facts
| Drug name | DOXYCYCLINE HYCLATE |
|---|---|
| Active ingredients | DOXYCYCLINE HYCLATE |
| Application type | ANDA |
| Application number | 208741 |
| Company | LUPIN |
| Dosage forms | TABLET, DELAYED RELEASE, ORAL |
| Strength | EQ 50MG BASE |
| Marketing status | Discontinued |
| TE codes | AB |
| Reference listed drug | No |
| Latest submission status date | Aug 11, 2023 |
At a glance
- 1–9 Submissions
- None Label versions
- 1–9 Products
- 1–9 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.