Drug application
BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE (BUPRENORPHINE HYDROCHLORIDE, NALOXONE HYDROCHLORIDE)
Drugs@FDA ANDA 204383 · ACTAVIS LABS UT INC
Key facts
| Drug name | BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE |
|---|---|
| Active ingredients | BUPRENORPHINE HYDROCHLORIDE, NALOXONE HYDROCHLORIDE |
| Application type | ANDA |
| Application number | 204383 |
| Company | ACTAVIS LABS UT INC |
| Dosage forms | FILM, BUCCAL, SUBLINGUAL |
| Strength | EQ 8MG BASE;EQ 2MG BASE |
| Marketing status | None (Tentative Approval) |
| Reference listed drug | No |
| Latest submission status date | Oct 24, 2017 |
At a glance
- 1–9 Submissions
- None 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: