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FENTANYL CITRATE
FENTANYL CITRATE - 52533-024-04 - (FENTANYL CITRATE)
Drug Information of FENTANYL CITRATE
| Product NDC: | 52533-024 |
| Proprietary Name: | FENTANYL CITRATE |
| Non Proprietary Name: | FENTANYL CITRATE |
| Active Ingredient(s): | 10 ug/mL & nbsp; FENTANYL CITRATE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of FENTANYL CITRATE
| Product NDC: | 52533-024 |
| Labeler Name: | Cantrell Drug Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20120413 |
Package Information of FENTANYL CITRATE
| Package NDC: | 52533-024-04 |
| Package Description: | 50 mL in 1 SYRINGE, PLASTIC (52533-024-04) |
NDC Information of FENTANYL CITRATE
| NDC Code | 52533-024-04 |
| Proprietary Name | FENTANYL CITRATE |
| Package Description | 50 mL in 1 SYRINGE, PLASTIC (52533-024-04) |
| Product NDC | 52533-024 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | FENTANYL CITRATE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20120413 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Cantrell Drug Company |
| Substance Name | FENTANYL CITRATE |
| Strength Number | 10 |
| Strength Unit | ug/mL |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
