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01 1Advanced Accelerator Applications
02 1Novartis Pharmaceuticals Corporation
03 1TELIX INNOVATIONS
04 1Telix Pharmaceuticals
05 1UIHC PET IMAGING
06 2University of California
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01 4POWDER;INTRAVENOUS
02 3SOLUTION;INTRAVENOUS
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01 7RX
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01 1GALLIUM GA 68 EDOTREOTIDE
02 2GALLIUM GA 68 GOZETOTIDE
03 1GOZELLIX
04 1ILLUCCIX
05 1LOCAMETZ
06 1NETSPOT
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01 7USA
Regulatory Info : RX
Registration Country : USA
Brand Name : NETSPOT
Dosage Form : POWDER;INTRAVENOUS
Dosage Strength : 2.1-5.5mCi/ML
Packaging :
Approval Date : 2016-06-01
Application Number : 208547
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : LOCAMETZ
Dosage Form : POWDER;INTRAVENOUS
Dosage Strength : N/A
Packaging :
Approval Date : 2022-03-23
Application Number : 215841
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ILLUCCIX
Dosage Form : POWDER;INTRAVENOUS
Dosage Strength : N/A
Packaging :
Approval Date : 2021-12-17
Application Number : 214032
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : GALLIUM GA 68 GOZETOTIDE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : 0.5-5mCi/mL
Packaging :
Approval Date : 2020-12-01
Application Number : 212642
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : GALLIUM GA 68 GOZETOTIDE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : 0.5-5mCi/mL
Packaging :
Approval Date : 2020-12-01
Application Number : 212643
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : GALLIUM GA 68 EDOTREOTIDE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : 0.5-4mCi/ML
Packaging :
Approval Date : 2019-08-21
Application Number : 210828
Regulatory Info : RX
Registration Country : USA
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : RX
Registration Country : USA
Brand Name : GOZELLIX
Dosage Form : POWDER;INTRAVENOUS
Dosage Strength : N/A
Packaging :
Approval Date : 2025-03-20
Application Number : 219592
Regulatory Info : RX
Registration Country : USA
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF