AK-FLUOR

Product NDC
50090-4535
11-digit product format
500904535
Labeler code
50090
Product ID
50090-4535_b01d5ba3-edf0-414b-bebc-147c8a9e6c34
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
fluorescein sodium
Dosage form
INJECTION
Route
INTRAVENOUS
Labeler
A-S Medication Solutions
Application
NDA022186
Marketing category
NDA
Marketing start
2008-10-01
Marketing end
0000-00-00
Substance
FLUORESCEIN SODIUM
Active strength
100 mg/mL
Pharmacologic classes
Diagnostic Dye [EPC],Dyes [MoA]
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
8f43a274-9585-47cb-b427-0eb3e578384dProduct name120250623
4a998fa9-995e-4ea5-97ef-93a559305758Product name120200706
c94ccba7-2a03-4a3e-a891-d62a57340fb2Product name120180215

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50090-4535-0AK-FLUOR5 mL in 1 VIAL, SINGLE-DOSEINJECTION54

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50090-4535AK-FLUOR (FLUORESCEIN SODIUM) INJECTION [A-S MEDICATION SOLUTIONS]4Legacy NDC, 1 package rows20210417_e18fb095-d580-433c-88c5-f234f509a00f.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50090-4535-0500904535005 mL in 1 VIAL, SINGLE-DOSE (50090-4535-0) 5 ml2019-09-180000-00-00NoNoCurrent