| NDC Code: |
0517-0725 |
| Proprietary Name: |
Buprenorphine Hydrochloride |
| Suffix: |
|
| Non-Proprietary Name: |
Buprenorphine Hydrochloride |
| Dosage Form: |
INJECTION, SOLUTION |
| Method: |
INTRAMUSCULAR; INTRAVENOUS |
| Original Marketing Date: |
13-08-2010 |
| Category Name: |
ANDA |
| Application Number: |
ANDA078331 |
| Labeler: |
AMERICAN REGENT, INC. |
| Substance Name: |
BUPRENORPHINE HYDROCHLORIDE |
| Active Numerator Strength: |
.324 |
| Active Ingredient Unit: |
mg/mL |
| Pharm Classes: |
Partial Opioid Agonist [EPC],Partial Opioid Agonists [MoA] |
| DEA Schedule: |
CIII |
