Drug application
DEXMEDETOMIDINE HYDROCHLORIDE (DEXMEDETOMIDINE HYDROCHLORIDE)
Drugs@FDA ANDA 201072 · FRESENIUS KABI USA
Key facts
| Drug name | DEXMEDETOMIDINE HYDROCHLORIDE |
|---|---|
| Active ingredients | DEXMEDETOMIDINE HYDROCHLORIDE |
| Application type | ANDA |
| Application number | 201072 |
| Company | FRESENIUS KABI USA |
| Dosage forms | INJECTABLE, INJECTION |
| Strength | EQ 200MCG BASE/2ML (EQ 100MCG BASE/ML) |
| Marketing status | Prescription |
| TE codes | AP |
| Reference listed drug | No |
| Latest submission class | Not Applicable |
| Latest submission status date | Sep 18, 2015 |
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.