Drug application
ULTACAN (ARTICAINE HYDROCHLORIDE, EPINEPHRINE BITARTRATE)
Drugs@FDA ANDA 201751 · HANSAMED INC
Key facts
| Drug name | ULTACAN |
|---|---|
| Active ingredients | ARTICAINE HYDROCHLORIDE, EPINEPHRINE BITARTRATE |
| Application type | ANDA |
| Application number | 201751 |
| Company | HANSAMED INC |
| Dosage forms | INJECTABLE, INJECTION |
| Strength | 4%;EQ 0.0085MG BASE/1.7ML (4%; EQ 0.005MG BASE/ML) |
| Marketing status | Discontinued |
| Reference listed drug | No |
| Latest submission status date | Jul 11, 2017 |
At a glance
- 1–9 Submissions
- 1–9 Label versions
- 1–9 Products
- None Therapeutic equivalents
- Yes FDA letters on file
- No 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: