FUL-GLO - 17478-404-01 - (Fluorescein Sodium)

Alphabetical Index


Drug Information of FUL-GLO

Product NDC: 17478-404
Proprietary Name: FUL-GLO
Non Proprietary Name: Fluorescein Sodium
Active Ingredient(s): 1    mg/1 & nbsp;   Fluorescein Sodium
Administration Route(s): OPHTHALMIC
Dosage Form(s): STRIP
Coding System: National Drug Codes(NDC)

Labeler Information of FUL-GLO

Product NDC: 17478-404
Labeler Name: Akorn, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20040601

Package Information of FUL-GLO

Package NDC: 17478-404-01
Package Description: 100 APPLICATOR in 1 CARTON (17478-404-01) > 1 STRIP in 1 APPLICATOR

NDC Information of FUL-GLO

NDC Code 17478-404-01
Proprietary Name FUL-GLO
Package Description 100 APPLICATOR in 1 CARTON (17478-404-01) > 1 STRIP in 1 APPLICATOR
Product NDC 17478-404
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluorescein Sodium
Dosage Form Name STRIP
Route Name OPHTHALMIC
Start Marketing Date 20040601
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Akorn, Inc.
Substance Name D&C YELLOW NO. 8
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Diagnostic Dye [EPC],Dyes [MoA]

Complete Information of FUL-GLO


General Information