fludeoxyglucose f 18
Generic: fludeoxyglucose f-18
Labeler: uihc-p e t imaging centerDrug Facts
Product Profile
Brand Name
fludeoxyglucose f 18
Generic Name
fludeoxyglucose f-18
Labeler
uihc-p e t imaging center
Dosage Form
INJECTION
Routes
Active Ingredients
fludeoxyglucose f-18 300 mCi/mL
Manufacturer
Identifiers & Regulatory
Product NDC
24417-001
Product ID
24417-001_ea94086a-dfc3-31b1-e053-2a95a90abb8a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA203990
Listing Expiration
2026-12-31
Marketing Start
2011-12-12
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
24417001
Hyphenated Format
24417-001
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
ANDA203990 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 300 mCi/mL
Packaging
- 30 mL in 1 VIAL, GLASS (24417-001-30)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "ea94086a-dfc3-31b1-e053-2a95a90abb8a", "openfda": {"nui": ["N0000177914", "N0000000205"], "unii": ["0Z5B2CJX4D"], "spl_set_id": ["4842b836-1a7c-4417-ab8d-aa37bf7065f8"], "pharm_class_epc": ["Radioactive Diagnostic Agent [EPC]"], "pharm_class_moa": ["Radiopharmaceutical Activity [MoA]"], "manufacturer_name": ["UIHC-P E T IMAGING CENTER"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 mL in 1 VIAL, GLASS (24417-001-30)", "package_ndc": "24417-001-30", "marketing_start_date": "20111212"}], "brand_name": "FLUDEOXYGLUCOSE F 18", "product_id": "24417-001_ea94086a-dfc3-31b1-e053-2a95a90abb8a", "dosage_form": "INJECTION", "pharm_class": ["Radioactive Diagnostic Agent [EPC]", "Radiopharmaceutical Activity [MoA]"], "product_ndc": "24417-001", "generic_name": "FLUDEOXYGLUCOSE F-18", "labeler_name": "UIHC-P E T IMAGING CENTER", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FLUDEOXYGLUCOSE F 18", "active_ingredients": [{"name": "FLUDEOXYGLUCOSE F-18", "strength": "300 mCi/mL"}], "application_number": "ANDA203990", "marketing_category": "ANDA", "marketing_start_date": "20111212", "listing_expiration_date": "20261231"}