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01 2Strides Pharma (Cyprus) Limited

02 2Aguettant Laboratory

03 2Bayer Ab

04 5Vale Pharmaceuticals Ltd

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSynergice, a Strides Pharma initiative, is a new gen B2B platform for diverse portofolio needs.

Regulatory Info : Deregistered

Registration Country : Sweden

Ibuprofen Sodium Dihydrate

Brand Name : Ibuprofen Strides

Dosage Form : Film Coated Tablet

Dosage Strength : 200mg

Packaging :

Approval Date : 06/10/2020

Application Number : 20190402000099

Regulatory Info : Deregistered

Registration Country : Sweden

Strides Pharma Science

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSynergice, a Strides Pharma initiative, is a new gen B2B platform for diverse portofolio needs.

Regulatory Info : Deregistered

Registration Country : Sweden

Ibuprofen Sodium Dihydrate

Brand Name : Ibuprofen Strides

Dosage Form : Film Coated Tablet

Dosage Strength : 400mg

Packaging :

Approval Date : 06/10/2020

Application Number : 20190402000105

Regulatory Info : Deregistered

Registration Country : Sweden

Strides Pharma Science

03

Aus. Peptide Conference
Not Confirmed
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Aus. Peptide Conference
Not Confirmed

Ibuprofen Sodium Dihydrate; Paracetamol

Brand Name : Comboval

Dosage Form : Infusion Solution

Dosage Strength : 10mg/ml ;3mg/ml

Packaging :

Approval Date : 29/06/2021

Application Number : 20200803000076

Regulatory Info : Approved

Registration Country : Sweden

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04

Aus. Peptide Conference
Not Confirmed
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Aus. Peptide Conference
Not Confirmed

Ibuprofen Sodium Dihydrate

Brand Name : Ibuprofen Bayer

Dosage Form : Film Coated Tablet

Dosage Strength : 200mg

Packaging :

Approval Date : 02/02/2007

Application Number : 20050316000052

Regulatory Info : Deregistered

Registration Country : Sweden

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05

Aus. Peptide Conference
Not Confirmed
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Aus. Peptide Conference
Not Confirmed

Ibuprofen Sodium Dihydrate

Brand Name : Ibuprofen Bayer

Dosage Form : Film Coated Tablet

Dosage Strength : 400mg

Packaging :

Approval Date : 02/02/2007

Application Number : 20050316000069

Regulatory Info : Deregistered

Registration Country : Sweden

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06

Vale Pharmaceuticals Ltd

Country
Aus. Peptide Conference
Not Confirmed
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Vale Pharmaceuticals Ltd

Country
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Aus. Peptide Conference
Not Confirmed

Ibuprofen Sodium Dihydrate; Paracetamol

Brand Name : Duofen

Dosage Form : Infusion Solution

Dosage Strength : 10mg/ml ;3mg/ml

Packaging :

Approval Date : 29/06/2021

Application Number : 20200803000083

Regulatory Info : Approved

Registration Country : Sweden

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07

Vale Pharmaceuticals Ltd

Country
Aus. Peptide Conference
Not Confirmed
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Vale Pharmaceuticals Ltd

Country
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Aus. Peptide Conference
Not Confirmed

Ibuprofen Sodium Dihydrate; Paracetamol

Brand Name : Paracetamol/Ibuprofen Vale

Dosage Form : Infusion Solution

Dosage Strength : 10mg/ml;3mg/ml

Packaging :

Approval Date : 30/07/2020

Application Number : 20190416000023

Regulatory Info : Approved

Registration Country : Sweden

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08

Vale Pharmaceuticals Ltd

Country
Aus. Peptide Conference
Not Confirmed
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Vale Pharmaceuticals Ltd

Country
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Aus. Peptide Conference
Not Confirmed

Ibuprofen Sodium Dihydrate; Paracetamol

Brand Name : Paracetamol/Ibuprofen Vale Pharma

Dosage Form : Infusion Solution

Dosage Strength : 10mg/ml;3mg/ml

Packaging :

Approval Date : 30/07/2020

Application Number : 20190416000054

Regulatory Info : Approved

Registration Country : Sweden

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09

Vale Pharmaceuticals Ltd

Country
Aus. Peptide Conference
Not Confirmed
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Vale Pharmaceuticals Ltd

Country
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Aus. Peptide Conference
Not Confirmed

Ibuprofen Sodium Dihydrate; Paracetamol

Brand Name : Paraibucomb

Dosage Form : Infusion Solution

Dosage Strength : 10mg/ml;3mg/ml

Packaging :

Approval Date : 30/07/2020

Application Number : 20190416000047

Regulatory Info : Approved

Registration Country : Sweden

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10

Vale Pharmaceuticals Ltd

Country
Aus. Peptide Conference
Not Confirmed
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Vale Pharmaceuticals Ltd

Country
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Aus. Peptide Conference
Not Confirmed

Ibuprofen Sodium Dihydrate; Paracetamol

Brand Name : Comboleve

Dosage Form : Infusion Solution

Dosage Strength : 10mg/ml;3mg/ml

Packaging :

Approval Date : 30/07/2020

Application Number : 20190416000030

Regulatory Info : Deregistered

Registration Country : Sweden

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