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01 2Sanofi-Aventis Ab

02 23M Deutschland Gmbh

03 1Cherubino Limited

04 2Clarben Sa Laboratories

05 2Farmalider Sa

06 4GALENICA SENESE Srl

07 2Inibsa Laboratories Sa

08 2Laboratorios Inibsa S.A.

09 2Laboratorios Inibsa, S.A.

10 2Laboratorios Inibsa, Sa

11 2Laboratorios Normon, Sa

12 4Materia Medica Maibach Ag

13 3Medius Ag

14 2Molteni Dental Srl

15 4Normon Laboratories Sa

16 2Pierrel Spa

17 10Septodont

18 2Septodont Ou Septodont Sas Ou Septodont Specialists

19 1Septodont Sas

20 2Streuli Pharma Ag

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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 : Deregistered

Registration Country : Sweden

Adrenaline; Articaine Hydrochloride

Brand Name : Ultracain

Dosage Form : Injectable Solution

Dosage Strength : 40mg/ml;10mcg/ml

Packaging :

Approval Date : 2011-12-09

Application Number : 20100803000086

Regulatory Info : Deregistered

Registration Country : Sweden

Sanofi Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info : Deregistered

Registration Country : Sweden

Adrenaline; Articaine Hydrochloride

Brand Name : Ultracain

Dosage Form : Injectable Solution

Dosage Strength : 40mg/ml;5mcg/ml

Packaging :

Approval Date : 2011-12-09

Application Number : 20100803000079

Regulatory Info : Deregistered

Registration Country : Sweden

Sanofi Company Banner

03

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

Adrenaline Hydrochloride; Articaine Hydrochloride

Brand Name : Ubistesin

Dosage Form : Injectable Solution

Dosage Strength : 40mg/ml;5mcg/ml

Packaging :

Approval Date : 2003-04-04

Application Number : 20030404000416

Regulatory Info : Deregistered

Registration Country : Sweden

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04

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

Adrenaline Hydrochloride; Articaine Hydrochloride

Brand Name : Ubistesin Forte

Dosage Form : Injectable Solution

Dosage Strength : 40mg/ml;10mcg/ml

Packaging :

Approval Date : 2003-04-04

Application Number : 20030404000423

Regulatory Info : Deregistered

Registration Country : Sweden

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05

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

Epinephrine Bitartrate; Articaine Hydrochloride

Brand Name : Articaina / Epinefrina Dermogen

Dosage Form : Injectable Solution

Dosage Strength : 40MG; 10MCG

Packaging :

Approval Date : 24-10-2006

Application Number : 68103

Regulatory Info : Authorized

Registration Country : Spain

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06

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

Epinephrine Bitartrate; Articaine Hydrochloride

Brand Name : Articaina / Epinefrina Dermogen

Dosage Form : Injectable Solution

Dosage Strength : 40MG; 5MCG

Packaging :

Approval Date : 24-10-2006

Application Number : 68104

Regulatory Info : Authorized

Registration Country : Spain

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07

ASPEN
Not Confirmed
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ASPEN
Not Confirmed

ARTICAINE HYDROCHLORIDE; Adrenaline Bitartrate

Brand Name : Sarticain

Dosage Form :

Dosage Strength : 10 Vials 20 Ml With Adrenaline 1:100,000  

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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08

Cherubino Limited

Country
ASPEN
Not Confirmed
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Cherubino Limited

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ASPEN
Not Confirmed

Articaine Hydrochloride; Adrenaline

Brand Name : Artinibsa

Dosage Form : Solution For Injection

Dosage Strength : 40MG/ML; 10MG/ML

Packaging :

Approval Date : 2024-06-28

Application Number :

Regulatory Info : Authorised

Registration Country : Malta

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09

Clarben Sa Laboratories

Country
ASPEN
Not Confirmed
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Clarben Sa Laboratories

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ASPEN
Not Confirmed

Epinephrine Bitartrate; Articaine Hydrochloride

Brand Name : Meganest

Dosage Form : Injectable Solution

Dosage Strength : 40MG; 10MCG

Packaging :

Approval Date : 01-06-1996

Application Number : 61194

Regulatory Info : Authorized

Registration Country : Spain

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10

Clarben Sa Laboratories

Country
ASPEN
Not Confirmed
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Clarben Sa Laboratories

Country
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ASPEN
Not Confirmed

Epinephrine Bitartrate; Articaine Hydrochloride

Brand Name : Meganest

Dosage Form : Injectable Solution

Dosage Strength : 40MG; 5MCG

Packaging :

Approval Date : 01-06-1996

Application Number : 61195

Regulatory Info : Authorized

Registration Country : Spain

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