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NDC 51754-2160-04 Fentanyl Citrate 50 ug/mL Details
Fentanyl Citrate 50 ug/mL
Fentanyl Citrate is a INTRAVENOUS INJECTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Exela Pharma Sciences, LLC. The primary component is FENTANYL CITRATE.
Product Information
NDC | 51754-2160 |
---|---|
Product ID | 51754-2160_e8e80dc7-fa22-4dff-95d6-299a579fd0a3 |
Associated GPIs | |
GCN Sequence Number | n/a |
GCN Sequence Number Description | n/a |
HIC3 | n/a |
HIC3 Description | n/a |
GCN | n/a |
HICL Sequence Number | n/a |
HICL Sequence Number Description | n/a |
Brand/Generic | n/a |
Proprietary Name | Fentanyl Citrate |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Fentanyl Citrate |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | INJECTION |
Route | INTRAVENOUS |
Active Ingredient Strength | 50 |
Active Ingredient Units | ug/mL |
Substance Name | FENTANYL CITRATE |
Labeler Name | Exela Pharma Sciences, LLC |
Pharmaceutical Class | Full Opioid Agonists [MoA], Opioid Agonist [EPC] |
DEA Schedule | CII |
Marketing Category | NDA |
Application Number | NDA215870 |
Listing Certified Through | 2024-12-31 |
Package
NDC 51754-2160-04 (51754216004)
NDC Package Code | 51754-2160-4 |
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Billing NDC | 51754216004 |
Package | 25 VIAL in 1 CARTON (51754-2160-4) / 100 mL in 1 VIAL (51754-2160-1) |
Marketing Start Date | 2023-05-01 |
NDC Exclude Flag | N |
Pricing Information | N/A |