Product NDC: | 52533-025 |
Proprietary Name: | Fentanyl Citrate |
Non Proprietary Name: | Fentanyl Citrate |
Active Ingredient(s): | 20 ug/mL & nbsp; Fentanyl Citrate |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52533-025 |
Labeler Name: | Cantrell Drug Company |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20130130 |
Package NDC: | 52533-025-75 |
Package Description: | 100 mL in 1 BAG (52533-025-75) |
NDC Code | 52533-025-75 |
Proprietary Name | Fentanyl Citrate |
Package Description | 100 mL in 1 BAG (52533-025-75) |
Product NDC | 52533-025 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Fentanyl Citrate |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20130130 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Cantrell Drug Company |
Substance Name | FENTANYL CITRATE |
Strength Number | 20 |
Strength Unit | ug/mL |
Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |