fentanyl citrate
Generic: fentanyl citrate
Labeler: fresenius kabi usa, llcDrug Facts
Product Profile
Brand Name
fentanyl citrate
Generic Name
fentanyl citrate
Labeler
fresenius kabi usa, llc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
fentanyl citrate 50 ug/mL
Manufacturer
Identifiers & Regulatory
Product NDC
63323-808
Product ID
63323-808_a47a3a31-e293-49d5-b6bc-950303525a64
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA212086
DEA Schedule
cii
Listing Expiration
2026-12-31
Marketing Start
2020-09-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63323808
Hyphenated Format
63323-808
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
fentanyl citrate (source: ndc)
Generic Name
fentanyl citrate (source: ndc)
Application Number
ANDA212086 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 ug/mL
Packaging
- 10 SYRINGE in 1 CARTON (63323-808-11) / 1 mL in 1 SYRINGE (63323-808-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "a47a3a31-e293-49d5-b6bc-950303525a64", "openfda": {"unii": ["MUN5LYG46H"], "rxcui": ["2474267", "2474269"], "spl_set_id": ["0c10e465-4117-48ba-a454-23ccb7a3fcc7"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 SYRINGE in 1 CARTON (63323-808-11) / 1 mL in 1 SYRINGE (63323-808-01)", "package_ndc": "63323-808-11", "marketing_start_date": "20200930"}], "brand_name": "Fentanyl Citrate", "product_id": "63323-808_a47a3a31-e293-49d5-b6bc-950303525a64", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "63323-808", "dea_schedule": "CII", "generic_name": "Fentanyl Citrate", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fentanyl Citrate", "active_ingredients": [{"name": "FENTANYL CITRATE", "strength": "50 ug/mL"}], "application_number": "ANDA212086", "marketing_category": "ANDA", "marketing_start_date": "20200930", "listing_expiration_date": "20261231"}