| NDC Code: |
16590-556 |
| Proprietary Name: |
PENTAZOCINE HCL AND NALOXONE HCL |
| Suffix: |
|
| Non-Proprietary Name: |
PENTAZOCINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE |
| Dosage Form: |
TABLET |
| Method: |
ORAL |
| Original Marketing Date: |
21-01-1997 |
| Category Name: |
ANDA |
| Application Number: |
ANDA074736 |
| Labeler: |
STAT RX USA LLC |
| Substance Name: |
NALOXONE HYDROCHLORIDE; PENTAZOCINE HYDROCHLORIDE |
| Active Numerator Strength: |
.5; 50 |
| Active Ingredient Unit: |
mg/1; mg/1 |
| Pharm Classes: |
Competitive Opioid Antagonists [MoA],Partial Opioid Agonist/Antagonist [EPC],Partial Opioid Agonists [MoA],Opioid Antagonist [EPC],Opioid Antagonists [MoA] |
| DEA Schedule: |
CIV |
