FdaApplication
ANDA 204383
Identifiers
- fda_app_no: ANDA204383
Properties
| Property | Value |
|---|---|
| applicant_name | ACTAVIS LABS UT INC |
| application_type | ANDA |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE | BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE | EQ 8MG BASE;EQ 2MG BASE | FILM;BUCCAL, SUBLINGUAL |
1 product