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NDC 00409-9093-35 Fentanyl Citrate 50 ug/mL Details
Fentanyl Citrate 50 ug/mL
Fentanyl Citrate is a INTRAMUSCULAR; INTRAVENOUS INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Hospira, Inc.. The primary component is FENTANYL CITRATE.
Product Information
| NDC | 00409-9093 |
|---|---|
| Product ID | 0409-9093_dd044413-7ca2-42d5-8d0d-781d2db4982c |
| Associated GPIs | 65100025102012 65100025102022 |
| GCN Sequence Number | 041384 |
| GCN Sequence Number Description | fentanyl citrate/PF AMPUL 50 MCG/ML INJECTION |
| HIC3 | H3H |
| HIC3 Description | OPIOID ANALGESIC, ANESTHETIC ADJUNCT AGENTS |
| GCN | 32806 |
| HICL Sequence Number | 025386 |
| HICL Sequence Number Description | FENTANYL CITRATE/PF |
| Brand/Generic | Generic |
| Proprietary Name | Fentanyl Citrate |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | FENTANYL CITRATE |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | INJECTION, SOLUTION |
| Route | INTRAMUSCULAR; INTRAVENOUS |
| Active Ingredient Strength | 50 |
| Active Ingredient Units | ug/mL |
| Substance Name | FENTANYL CITRATE |
| Labeler Name | Hospira, Inc. |
| Pharmaceutical Class | Full Opioid Agonists [MoA], Opioid Agonist [EPC] |
| DEA Schedule | CII |
| Marketing Category | NDA |
| Application Number | NDA019115 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 00409-9093-35 (00409909335)
| NDC Package Code | 0409-9093-35 |
|---|---|
| Billing NDC | 00409909335 |
| Package | 10 AMPULE in 1 CELLO PACK (0409-9093-35) / 5 mL in 1 AMPULE (0409-9093-45) |
| Marketing Start Date | 2005-12-14 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |