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01 1Sanofi

02 1Lotus Pharmaceutical Industries

03 5VALIDUS PHARMS

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American Pharma Summit
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  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

Regulatory Info : Generic

Registration Country : South Africa

Dolasetron Mesylate

Brand Name : Zamanon 100 mg IV

Dosage Form : INJ

Dosage Strength : 5mg/ml

Packaging : 1X1mg/ml

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : South Africa

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02

American Pharma Summit
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American Pharma Summit
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Dolasetron Mesylate

Brand Name :

Dosage Form : Injection

Dosage Strength : 12.5MG/0.625ML

Packaging : Vial

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : Egypt

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03

American Pharma Summit
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American Pharma Summit
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DOLASETRON MESYLATE

Brand Name : ANZEMET

Dosage Form : TABLET;ORAL

Dosage Strength : 50MG

Packaging :

Approval Date : 1997-09-11

Application Number : 20623

Regulatory Info : DISCN

Registration Country : USA

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04

American Pharma Summit
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American Pharma Summit
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DOLASETRON MESYLATE

Brand Name : ANZEMET

Dosage Form : TABLET;ORAL

Dosage Strength : 100MG

Packaging :

Approval Date : 1997-09-11

Application Number : 20623

Regulatory Info : DISCN

Registration Country : USA

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05

American Pharma Summit
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American Pharma Summit
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DOLASETRON MESYLATE

Brand Name : ANZEMET

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 100MG/5ML (20MG/ML)

Packaging :

Approval Date : 1997-09-11

Application Number : 20624

Regulatory Info : DISCN

Registration Country : USA

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06

American Pharma Summit
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American Pharma Summit
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DOLASETRON MESYLATE

Brand Name : ANZEMET

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 12.5MG/0.625ML (20MG/ML)

Packaging :

Approval Date : 1997-09-11

Application Number : 20624

Regulatory Info : DISCN

Registration Country : USA

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07

American Pharma Summit
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American Pharma Summit
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DOLASETRON MESYLATE

Brand Name : ANZEMET

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 500MG/25ML (20MG/ML)

Packaging :

Approval Date : 2001-12-11

Application Number : 20624

Regulatory Info : DISCN

Registration Country : USA

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