fludeoxyglucose f 18
Generic: fludeoxyglucose f 18
Labeler: sofie co. dba sofieDrug Facts
Product Profile
Brand Name
fludeoxyglucose f 18
Generic Name
fludeoxyglucose f 18
Labeler
sofie co. dba sofie
Dosage Form
INJECTION
Routes
Active Ingredients
fludeoxyglucose f-18 20 mCi/mL
Manufacturer
Identifiers & Regulatory
Product NDC
73410-003
Product ID
73410-003_34012195-5fcd-eff1-e063-6294a90a98de
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA204463
Listing Expiration
2026-12-31
Marketing Start
2019-11-06
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
73410003
Hyphenated Format
73410-003
Supplemental Identifiers
UNII
NUI
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
fludeoxyglucose f 18 (source: ndc)
Generic Name
fludeoxyglucose f 18 (source: ndc)
Application Number
ANDA204463 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mCi/mL
Packaging
- 30 mL in 1 VIAL, MULTI-DOSE (73410-003-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "34012195-5fcd-eff1-e063-6294a90a98de", "openfda": {"nui": ["N0000177914", "N0000000205"], "unii": ["0Z5B2CJX4D"], "spl_set_id": ["915b1f71-616d-4cd9-90a7-bc556736a3d1"], "pharm_class_epc": ["Radioactive Diagnostic Agent [EPC]"], "pharm_class_moa": ["Radiopharmaceutical Activity [MoA]"], "manufacturer_name": ["SOFIE Co. dba SOFIE"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 mL in 1 VIAL, MULTI-DOSE (73410-003-01)", "package_ndc": "73410-003-01", "marketing_start_date": "20191106"}], "brand_name": "Fludeoxyglucose F 18", "product_id": "73410-003_34012195-5fcd-eff1-e063-6294a90a98de", "dosage_form": "INJECTION", "pharm_class": ["Radioactive Diagnostic Agent [EPC]", "Radiopharmaceutical Activity [MoA]"], "product_ndc": "73410-003", "generic_name": "Fludeoxyglucose F 18", "labeler_name": "SOFIE Co. dba SOFIE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fludeoxyglucose F 18", "active_ingredients": [{"name": "FLUDEOXYGLUCOSE F-18", "strength": "20 mCi/mL"}], "application_number": "ANDA204463", "marketing_category": "ANDA", "marketing_start_date": "20191106", "listing_expiration_date": "20261231"}