Drug application
DURANEST (EPINEPHRINE BITARTRATE, ETIDOCAINE HYDROCHLORIDE)
Drugs@FDA NDA 021384 · DENTSPLY PHARM
Key facts
| Drug name | DURANEST |
|---|---|
| Active ingredients | EPINEPHRINE BITARTRATE, ETIDOCAINE HYDROCHLORIDE |
| Application type | NDA |
| Application number | 021384 |
| Company | DENTSPLY PHARM |
| Dosage forms | INJECTABLE, INJECTION |
| Strength | 0.005MG/ML;1.5% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
| Marketing status | Discontinued |
| Reference listed drug | Yes |
| Latest submission status date | Aug 30, 1976 |
At a glance
- 1–9 Submissions
- None Label versions
- 1–9 Products
- None 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.