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01 1Sanofi

02 1Eli Lilly

03 1Ferring Pharmaceuticals

04 1Sun Pharmaceutical Industries Limited

05 2Teva Pharmaceutical Industries

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info : DISCN

Registration Country : USA

TERIPARATIDE ACETATE

Brand Name : PARATHAR

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 200 UNITS/VIAL

Packaging :

Approval Date : 1987-12-23

Application Number : 19498

Regulatory Info : DISCN

Registration Country : USA

Sanofi Company Banner

02

World Health Expo
Not Confirmed
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World Health Expo
Not Confirmed

Parathar Acetate

Brand Name : Forsteo

Dosage Form : Teriparatide 600Mcg 2,4Ml Parenteral Use

Dosage Strength : 1 pen SC 2.4 ml 20 mcg/80 mcl

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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03

World Health Expo
Not Confirmed
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World Health Expo
Not Confirmed

Terlipressin Acetate

Brand Name : Glypressin

Dosage Form : Powder And Solvents For Solution For Injection

Dosage Strength :

Packaging :

Approval Date : 19-09-1996

Application Number : 28101805996

Regulatory Info : Prescription

Registration Country : Denmark

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04

World Health Expo
Not Confirmed
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World Health Expo
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Terlipressin Acetate

Brand Name : Terlipressinacetat \"Sun\"

Dosage Form : Injection Solution

Dosage Strength :

Packaging :

Approval Date : 06-12-2012

Application Number : 28104939711

Regulatory Info : Prescription

Registration Country : Denmark

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05

World Health Expo
Not Confirmed
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World Health Expo
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TERIPARATIDE (TERIPARATIDE ACETATE)

Brand Name : TEVA-TERIPARATIDE INJECTION

Dosage Form : SOLUTION

Dosage Strength : 250MCG/ML

Packaging :

Approval Date :

Application Number : 2486423

Regulatory Info : Prescription

Registration Country : Canada

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06

World Health Expo
Not Confirmed
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World Health Expo
Not Confirmed

Teriparatide Acetate

Brand Name : Tetridar

Dosage Form : Solution For Injection

Dosage Strength : 20mcg/80microlitre

Packaging :

Approval Date : 19-12-2017

Application Number : 28105994917

Regulatory Info : Prescription

Registration Country : Denmark

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