fentanyl citrate
Generic: fentanyl citrate
Labeler: hikma pharmaceuticals usa inc.Drug Facts
Product Profile
Brand Name
fentanyl citrate
Generic Name
fentanyl citrate
Labeler
hikma pharmaceuticals usa inc.
Dosage Form
INJECTION
Routes
Active Ingredients
fentanyl citrate 50 ug/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0641-6030
Product ID
0641-6030_a630adc0-2731-4d0b-b965-b846f45a9a75
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA019101
DEA Schedule
cii
Listing Expiration
2027-12-31
Marketing Start
1984-07-11
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
06416030
Hyphenated Format
0641-6030
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
NDA019101 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 ug/mL
Packaging
- 50 mL in 1 VIAL (0641-6030-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "a630adc0-2731-4d0b-b965-b846f45a9a75", "openfda": {"unii": ["MUN5LYG46H"], "rxcui": ["1735003", "1735007", "1735008", "1735013", "2168270", "2474269", "2629337"], "spl_set_id": ["ce5db1c2-feb1-4ad2-847a-d02e865bd47e"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 VIAL (0641-6030-01)", "package_ndc": "0641-6030-01", "marketing_start_date": "19840711"}], "brand_name": "Fentanyl Citrate", "product_id": "0641-6030_a630adc0-2731-4d0b-b965-b846f45a9a75", "dosage_form": "INJECTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0641-6030", "dea_schedule": "CII", "generic_name": "Fentanyl Citrate", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fentanyl Citrate", "active_ingredients": [{"name": "FENTANYL CITRATE", "strength": "50 ug/mL"}], "application_number": "NDA019101", "marketing_category": "NDA", "marketing_start_date": "19840711", "listing_expiration_date": "20271231"}