Product NDC: | 0409-1465 |
Proprietary Name: | Nalbuphine Hydrochloride |
Non Proprietary Name: | NALBUPHINE HYDROCHLORIDE |
Active Ingredient(s): | 20 mg/mL & nbsp; NALBUPHINE HYDROCHLORIDE |
Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0409-1465 |
Labeler Name: | Hospira, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA070916 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110822 |
Package NDC: | 0409-1465-61 |
Package Description: | 10 AMPULE in 1 CARTON (0409-1465-61) > 1 mL in 1 AMPULE |
NDC Code | 0409-1465-61 |
Proprietary Name | Nalbuphine Hydrochloride |
Package Description | 10 AMPULE in 1 CARTON (0409-1465-61) > 1 mL in 1 AMPULE |
Product NDC | 0409-1465 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | NALBUPHINE HYDROCHLORIDE |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
Start Marketing Date | 20110822 |
Marketing Category Name | ANDA |
Labeler Name | Hospira, Inc. |
Substance Name | NALBUPHINE HYDROCHLORIDE |
Strength Number | 20 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Competitive Opioid Antagonists [MoA],Opioid Agonist/Antagonist [EPC],Partial Opioid Agonists [MoA] |