Sodium Fluoride F 18

Product NDC
24562-002
11-digit product format
245620002
Labeler code
24562
Product ID
24562-002_2fa616a8-a06e-4fd6-b003-ef8935b5d8d0
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
SODIUM FLUORIDE F-18
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Labeler
Biomedical Research Foundation of Northwest Louisiana
Application
ANDA204351
Marketing category
ANDA
Marketing start
2015-01-22
Substance
SODIUM FLUORIDE F-18
Active strength
200 mCi/mL
Pharmacologic classes
Radioactive Diagnostic Agent [EPC], Radiopharmaceutical Activity [MoA]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Sodium Fluoride F 18
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SODIUM FLUORIDE F-18200 mCi/mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii9L75099X6R

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
2d79dac3-9c48-45b0-a9b7-a8ef22ff9f55Product name120151112
9209e30a-83c7-4466-acf0-7533654a2b1cProduct name920151029

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
24562-002-30Sodium Fluoride F 1830 mL in 1 VIAL, MULTI-DOSEINJECTION, SOLUTION307

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
24562-002SODIUM FLUORIDE F 18 (SODIUM FLUORIDE F-18) INJECTION, SOLUTION [BIOMEDICAL RESEARCH FOUNDATION OF NORTHWEST LOUISIANA]6Current NDC, Legacy NDC, 1 package rows20230211_4c45fe05-e3b7-4383-966c-4e218ff6f94a.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
24562-002-302456200023030 mL in 1 VIAL, MULTI-DOSE (24562-002-30) 30 ml2015-01-220000-00-00NoNoCurrent