Drug application
TOFRANIL (IMIPRAMINE HYDROCHLORIDE)
Drugs@FDA NDA 011838 · NOVARTIS
Key facts
| Drug name | TOFRANIL |
|---|---|
| Active ingredients | IMIPRAMINE HYDROCHLORIDE |
| Application type | NDA |
| Application number | 011838 |
| Company | NOVARTIS |
| Dosage forms | INJECTABLE, INJECTION |
| Strength | 12.5MG/ML |
| Marketing status | Discontinued |
| Reference listed drug | No |
| Latest submission class | Type 3 - New Dosage Form |
| Latest submission status date | Oct 2, 1959 |
At a glance
- 1–9 Submissions
- 10–99 Supplements
- None Label versions
- 1–9 Products
- None Therapeutic equivalents
- No 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: