Fentanyl Citrate is a Intramuscular; Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Fresenius Kabi Usa, Llc. The primary component is Fentanyl Citrate.
Product ID | 63323-806_23c7a740-61c9-488d-8041-bbb2e85016ac |
NDC | 63323-806 |
Product Type | Human Prescription Drug |
Proprietary Name | Fentanyl Citrate |
Generic Name | Fentanyl Citrate |
Dosage Form | Injection, Solution |
Route of Administration | INTRAMUSCULAR; INTRAVENOUS |
Marketing Start Date | 2019-05-03 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA210762 |
Labeler Name | Fresenius Kabi USA, LLC |
Substance Name | FENTANYL CITRATE |
Active Ingredient Strength | 0 mg/mL |
Pharm Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
DEA Schedule | CII |
NDC Exclude Flag | N |
Listing Certified Through | 2022-12-31 |
Marketing Start Date | 2019-05-03 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | ANDA |
Application Number | ANDA210762 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2019-05-03 |
Marketing Category | ANDA |
Application Number | ANDA210762 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2019-05-03 |
Marketing Category | ANDA |
Application Number | ANDA210762 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2019-05-03 |
Marketing Category | ANDA |
Application Number | ANDA210762 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2019-05-03 |
Marketing Category | ANDA |
Application Number | ANDA210762 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2019-05-03 |
Marketing Category | ANDA |
Application Number | ANDA210762 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2019-05-03 |
Marketing Category | ANDA |
Application Number | ANDA210762 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2019-05-03 |
Marketing Category | ANDA |
Application Number | ANDA210762 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2019-05-03 |
Marketing Category | ANDA |
Application Number | ANDA210762 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2019-05-03 |
Ingredient | Strength |
---|---|
FENTANYL CITRATE | .05 mg/mL |
SPL SET ID: | 38d0c14a-a0c1-44cc-a939-0304eb8037d6 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
0093-7865 | Fentanyl Citrate | Fentanyl Citrate |
0093-7866 | Fentanyl Citrate | Fentanyl Citrate |
0093-7867 | Fentanyl Citrate | Fentanyl Citrate |
0093-7868 | Fentanyl Citrate | Fentanyl Citrate |
0093-7869 | Fentanyl Citrate | Fentanyl Citrate |
0093-7870 | Fentanyl Citrate | Fentanyl Citrate |
0406-9202 | FENTANYL CITRATE | FENTANYL CITRATE |
0409-9093 | FENTANYL CITRATE | FENTANYL CITRATE |
0409-9094 | Fentanyl Citrate | Fentanyl Citrate |
0641-6024 | Fentanyl Citrate | Fentanyl Citrate |
0641-6026 | Fentanyl Citrate | Fentanyl Citrate |
0641-6028 | Fentanyl Citrate | Fentanyl Citrate |
0641-6029 | Fentanyl Citrate | Fentanyl Citrate |
0641-6030 | Fentanyl Citrate | Fentanyl Citrate |
0641-6025 | Fentanyl Citrate | Fentanyl Citrate |
0641-6027 | Fentanyl Citrate | Fentanyl Citrate |
17478-030 | FENTANYL CITRATE | FENTANYL CITRATE |
17478-031 | FENTANYL CITRATE | FENTANYL CITRATE |
52533-074 | Fentanyl Citrate | Fentanyl Citrate |
52533-025 | Fentanyl Citrate | Fentanyl Citrate |
52533-214 | FENTANYL CITRATE | FENTANYL CITRATE |
0406-9216 | FENTANYL CITRATE | FENTANYL CITRATE |
0406-9204 | FENTANYL CITRATE | FENTANYL CITRATE |
0406-9206 | FENTANYL CITRATE | FENTANYL CITRATE |
0406-9208 | FENTANYL CITRATE | FENTANYL CITRATE |
0406-9212 | FENTANYL CITRATE | FENTANYL CITRATE |
0409-1276 | Fentanyl Citrate | Fentanyl Citrate |
63323-806 | Fentanyl Citrate | Fentanyl Citrate |