NDC Code | 51662-1420-1 |
Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (51662-1420-1) > 10 mL in 1 VIAL, MULTI-DOSE |
Product NDC | 51662-1420 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Nalbuphine Hci |
Non-Proprietary Name | Nalbuphine Hci |
Dosage Form | INJECTION, SOLUTION |
Usage | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
Start Marketing Date | 20191029 |
Marketing Category Name | ANDA |
Application Number | ANDA070915 |
Manufacturer | HF Acquisition Co LLC, DBA HealthFirst |
Substance Name | NALBUPHINE HYDROCHLORIDE |
Strength | 10 |
Strength Unit | mg/mL |
Pharmacy Classes | Competitive Opioid Antagonists [MoA], Opioid Agonist/Antagonist [EPC], Partial Opioid Agonists [MoA] |