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01 1BICISATE DIHYDROCHLORIDE

02 2GADOFOSVESET TRISODIUM

03 1GALLIUM CITRATE GA-67

04 3PERFLUTREN

05 1SAMARIUM SM-153 LEXIDRONAM PENTASODIUM

06 1TECHNETIUM TC 99M

07 1TECHNETIUM TC-99M BICISATE KIT

08 2TECHNETIUM TC-99M SESTAMIBI KIT

09 2TECHNETIUM TC-99M SODIUM PERTECHNETATE GENERATOR

10 1TETRAKIS [CU(MIBI)4]BF4

11 2THALLOUS CHLORIDE TL-201

12 3XENON XE-133

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PharmaCompass

01

Brand Name : NEUROLITE

Pharma, Lab & Chemical Expo
Not Confirmed
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Brand Name : NEUROLITE

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Pharma, Lab & Chemical Expo
Not Confirmed

Lantheus Medical Imaging

Dosage Form : KIT

Brand Name : NEUROLITE

Dosage Strength : 0.9MG/VIAL

Packaging : 2 OR 5 KITS (VIAL A AND VIAL B)

Approval Date :

Application Number : 2327848

Regulatory Info : Schedule C

Registration Country : Canada

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02

Brand Name : ABLAVAR

Pharma, Lab & Chemical Expo
Not Confirmed
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Brand Name : ABLAVAR

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Pharma, Lab & Chemical Expo
Not Confirmed

Lantheus Medical Imaging

Dosage Form : SOLUTION;INTRAVENOUS

Brand Name : ABLAVAR

Dosage Strength : 2440MG/10ML (244MG/ML)

Packaging :

Approval Date : 2008-12-22

Application Number : 21711

Regulatory Info : DISCN

Registration Country : USA

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03

Brand Name : ABLAVAR

Pharma, Lab & Chemical Expo
Not Confirmed
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Brand Name : ABLAVAR

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Pharma, Lab & Chemical Expo
Not Confirmed

Lantheus Medical Imaging

Dosage Form : SOLUTION;INTRAVENOUS

Brand Name : ABLAVAR

Dosage Strength : 3660MG/15ML (244MG/ML)

Packaging :

Approval Date : 2008-12-22

Application Number : 21711

Regulatory Info : DISCN

Registration Country : USA

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04

Brand Name : GALLIUM CITRATE GA 6...

Pharma, Lab & Chemical Expo
Not Confirmed
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Brand Name : GALLIUM CITRATE GA 6...

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Pharma, Lab & Chemical Expo
Not Confirmed

Lantheus Medical Imaging

Dosage Form : INJECTABLE;INJECTION

Brand Name : GALLIUM CITRATE GA 67

Dosage Strength : 2mCi/ML

Packaging :

Approval Date : 1982-01-01

Application Number : 17478

Regulatory Info : DISCN

Registration Country : USA

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05

Brand Name : DEFINITY

Pharma, Lab & Chemical Expo
Not Confirmed
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Brand Name : DEFINITY

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Pharma, Lab & Chemical Expo
Not Confirmed

Lantheus Medical Imaging

Dosage Form : INJECTABLE;INTRAVENOUS

Brand Name : DEFINITY

Dosage Strength : 13.04MG/2ML (6.52MG/ML...

Packaging :

Approval Date : 2001-07-31

Application Number : 21064

Regulatory Info : RX

Registration Country : USA

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06

Brand Name : DEFINITY RT

Pharma, Lab & Chemical Expo
Not Confirmed
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Brand Name : DEFINITY RT

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Pharma, Lab & Chemical Expo
Not Confirmed

Lantheus Medical Imaging

Dosage Form : INJECTABLE;INTRAVENOUS

Brand Name : DEFINITY RT

Dosage Strength : 13.04MG/2ML (6.52MG/ML...

Packaging :

Approval Date : 2020-11-17

Application Number : 21064

Regulatory Info : RX

Registration Country : USA

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07

Brand Name : DEFINITY

Pharma, Lab & Chemical Expo
Not Confirmed
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Brand Name : DEFINITY

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Pharma, Lab & Chemical Expo
Not Confirmed

Lantheus Medical Imaging

Dosage Form : SUSPENSION

Brand Name : DEFINITY

Dosage Strength : 150MCL/ML

Packaging : 1.5ML

Approval Date :

Application Number : 2243173

Regulatory Info : Prescription

Registration Country : Canada

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08

Brand Name : QUADRAMET

Pharma, Lab & Chemical Expo
Not Confirmed
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Brand Name : QUADRAMET

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Pharma, Lab & Chemical Expo
Not Confirmed

Lantheus Medical Imaging

Dosage Form : INJECTABLE;INJECTION

Brand Name : QUADRAMET

Dosage Strength : 50mCi/ML

Packaging :

Approval Date : 1997-03-28

Application Number : 20570

Regulatory Info : DISCN

Registration Country : USA

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09

Brand Name : TECHNELITE

Pharma, Lab & Chemical Expo
Not Confirmed
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Brand Name : TECHNELITE

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Pharma, Lab & Chemical Expo
Not Confirmed

Lantheus Medical Imaging

Dosage Form : SOLUTION

Brand Name : TECHNELITE

Dosage Strength : 740GBQ/GEN

Packaging :

Approval Date :

Application Number : 2328550

Regulatory Info : Schedule C

Registration Country : Canada

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10

Brand Name : NEUROLITE

Pharma, Lab & Chemical Expo
Not Confirmed
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Brand Name : NEUROLITE

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Pharma, Lab & Chemical Expo
Not Confirmed

Lantheus Medical Imaging

Dosage Form : INJECTABLE;INJECTION

Brand Name : NEUROLITE

Dosage Strength : N/A

Packaging :

Approval Date : 1994-11-23

Application Number : 20256

Regulatory Info : RX

Registration Country : USA

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