Drug application
DOXEPIN HYDROCHLORIDE (DOXEPIN HYDROCHLORIDE)
Drugs@FDA ANDA 070791 · MYLAN PHARMS INC
Key facts
| Drug name | DOXEPIN HYDROCHLORIDE |
|---|---|
| Active ingredients | DOXEPIN HYDROCHLORIDE |
| Application type | ANDA |
| Application number | 070791 |
| Company | MYLAN PHARMS INC |
| Dosage forms | CAPSULE, ORAL |
| Strength | EQ 50MG BASE |
| Marketing status | Prescription |
| TE codes | AB |
| Reference listed drug | No |
| Latest submission status date | May 13, 1986 |
At a glance
- 1–9 Submissions
- 10–99 Supplements
- 1–9 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.
Source: U.S. Food and Drug Administration (FDA), Drugs@FDA · Source date: