01 1ALCON LABS INC
02 2LONG GROVE PHARMS
03 2NEXUS PHARMS
04 1NOVARTIS
01 1INJECTABLE;INJECTION
02 5INJECTABLE;INTRAVENOUS
01 1DISCN
02 5RX
01 1AK-FLUOR 10%
02 1AK-FLUOR 25%
03 2FLUORESCEIN SODIUM
04 1FLUORESCITE
05 1FUNDUSCEIN-25
01 2No
02 4Yes
RLD : Yes
TE Code : AP
Brand Name : FLUORESCITE
Dosage Form : INJECTABLE;INTRAVENOUS
Dosage Strength : EQ 500MG BASE/5ML (EQ 100MG BASE/ML)
Approval Date : 2006-03-28
Application Number : 21980
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AP
RLD : Yes
TE Code : AP
Brand Name : AK-FLUOR 10%
Dosage Form : INJECTABLE;INTRAVENOUS
Dosage Strength : EQ 500MG BASE/5ML (EQ 100MG BASE/ML)
Approval Date : 2008-08-08
Application Number : 22186
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AP
RLD : Yes
TE Code : AP
Brand Name : AK-FLUOR 25%
Dosage Form : INJECTABLE;INTRAVENOUS
Dosage Strength : EQ 500MG BASE/2ML (EQ 250MG BASE/ML)
Approval Date : 2008-08-08
Application Number : 22186
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AP
RLD : No
TE Code : AP
Brand Name : FLUORESCEIN SODIUM
Dosage Form : INJECTABLE;INTRAVENOUS
Dosage Strength : EQ 500MG BASE/5ML (EQ 100MG BASE/ML)
Approval Date : 2023-09-25
Application Number : 215709
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
RLD : No
TE Code : AP
Brand Name : FLUORESCEIN SODIUM
Dosage Form : INJECTABLE;INTRAVENOUS
Dosage Strength : EQ 500MG BASE/2ML (EQ 250MG BASE/ML)
Approval Date : 2023-09-25
Application Number : 215709
RX/OTC/DISCN : RX
RLD : No
TE Code : AP
RLD : Yes
TE Code :
Brand Name : FUNDUSCEIN-25
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 25% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 17869
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
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