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01 5Aspen Pharmacare Holdings

02 3Orion Corporation

03 3Actavis Inc

04 6B. Braun Medical

05 3B. Braun Melsungen AG

06 4Cristalia Produtos Quimicos Farma. Ltda

07 2Farmatek

08 3Fresenius Kabi USA

09 7GSK

10 3Hameln Pharma GmbH

11 3Hanlim Pharmaceuticals Inc

12 3Hikma Pharmaceuticals

13 6Hospira, Inc.

14 3Nivagen

15 3Pharma Dynamics

16 2STERIMAX INC

17 3Sandoz B2B

18 3Teva Pharmaceutical Industries

19 2Themis Medicare

20 3Viatris

21 3Viatris South Africa (Pty) Ltd

22 3Yichang Humanwell Pharmaceutical

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PharmaCompass

01

Remifentanil

Brand Name : Fortiva 1mg

Dosage Form : INJ

Dosage Strength : 1mg/3ml

Packaging : 3X5mg/3ml

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : South Africa

Aspen API Comapny Banner

02

remifentanilhydroklorid

Brand Name : Remifentanil Orion

Dosage Form : PULVER TILL KONCENTRAT TILL INJEKTIONS-

Dosage Strength : 2 MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

Fermion Orion Company Banner

03

Remifentanil

Brand Name : Fortiva 2mg

Dosage Form : INJ

Dosage Strength : 2mg/5ml

Packaging : 5X5mg/5ml

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : South Africa

Aspen API Comapny Banner

04

Remifentanil

Brand Name : Fortiva 5mg

Dosage Form : INJ

Dosage Strength : 5mg/10ml

Packaging : 10X5mg/10ml

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : South Africa

Aspen API Comapny Banner

05

Remifentanil

Brand Name : Ultiva 1 mg

Dosage Form : INJ

Dosage Strength : 1mg/3ml

Packaging : 3X5mg/3ml

Approval Date :

Application Number :

Regulatory Info : Originator

Registration Country : South Africa

Aspen API Comapny Banner

06

Remifentanil

Brand Name : Ultiva 2 mg

Dosage Form : INJ

Dosage Strength : 2mg/5ml

Packaging : 5X5mg/5ml

Approval Date :

Application Number :

Regulatory Info : Originator

Registration Country : South Africa

Aspen API Comapny Banner

07

remifentanilhydroklorid

Brand Name : Remifentanil Orion

Dosage Form : PULVER TILL KONCENTRAT TILL INJEKTIONS-

Dosage Strength : 5 MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

Fermion Orion Company Banner

08

remifentanilhydroklorid

Brand Name : Remifentanil Orion

Dosage Form : PULVER TILL KONCENTRAT TILL INJEKTIONS-

Dosage Strength : 1 MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Sweden

Fermion Orion Company Banner

09

Iran Expo
Not Confirmed
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Iran Expo
Not Confirmed

REMIFENTANIL HYDROCHLORIDE

Brand Name : REMIFENTANIL HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1MG BASE/VIAL

Packaging :

Approval Date : 2018-01-16

Application Number : 206223

Regulatory Info : RX

Registration Country : USA

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10

Iran Expo
Not Confirmed
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Iran Expo
Not Confirmed

REMIFENTANIL HYDROCHLORIDE

Brand Name : REMIFENTANIL HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 2MG BASE/VIAL

Packaging :

Approval Date : 2018-01-16

Application Number : 206223

Regulatory Info : RX

Registration Country : USA

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11

Iran Expo
Not Confirmed
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Iran Expo
Not Confirmed

REMIFENTANIL HYDROCHLORIDE

Brand Name : REMIFENTANIL HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 5MG BASE/VIAL

Packaging :

Approval Date : 2018-01-16

Application Number : 206223

Regulatory Info : RX

Registration Country : USA

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12

Iran Expo
Not Confirmed
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Iran Expo
Not Confirmed

REMIFENTANIL HYDROCHLORIDE

Brand Name : REMIFENTANIL HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1MG BASE/VIAL

Packaging :

Approval Date : 2020-10-13

Application Number : 210594

Regulatory Info : RX

Registration Country : USA

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13

Iran Expo
Not Confirmed
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Iran Expo
Not Confirmed

REMIFENTANIL HYDROCHLORIDE

Brand Name : REMIFENTANIL HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 2MG BASE/VIAL

Packaging :

Approval Date : 2020-10-13

Application Number : 210594

Regulatory Info : RX

Registration Country : USA

blank

14

Iran Expo
Not Confirmed
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Iran Expo
Not Confirmed

REMIFENTANIL HYDROCHLORIDE

Brand Name : REMIFENTANIL HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 5MG BASE/VIAL

Packaging :

Approval Date : 2020-10-13

Application Number : 210594

Regulatory Info : RX

Registration Country : USA

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15

Iran Expo
Not Confirmed
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Iran Expo
Not Confirmed

REMIFENTANIL HYDROCHLORIDE

Brand Name : REMIFENTANIL HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1MG BASE/VIAL

Packaging :

Approval Date : 2024-06-28

Application Number : 215635

Regulatory Info : RX

Registration Country : USA

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16

Iran Expo
Not Confirmed
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Iran Expo
Not Confirmed

REMIFENTANIL HYDROCHLORIDE

Brand Name : REMIFENTANIL HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 2MG BASE/VIAL

Packaging :

Approval Date : 2024-06-28

Application Number : 215635

Regulatory Info : RX

Registration Country : USA

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17

Iran Expo
Not Confirmed
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Iran Expo
Not Confirmed

REMIFENTANIL HYDROCHLORIDE

Brand Name : REMIFENTANIL HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 5MG BASE/VIAL

Packaging :

Approval Date : 2024-06-28

Application Number : 215635

Regulatory Info : RX

Registration Country : USA

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18

Iran Expo
Not Confirmed
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Iran Expo
Not Confirmed

REMIFENTANIL HYDROCHLORIDE

Brand Name : ULTIVA

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 1MG BASE/VIAL

Packaging :

Approval Date : 1996-07-12

Application Number : 20630

Regulatory Info : RX

Registration Country : USA

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19

Iran Expo
Not Confirmed
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Iran Expo
Not Confirmed

REMIFENTANIL HYDROCHLORIDE

Brand Name : ULTIVA

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 2MG BASE/VIAL

Packaging :

Approval Date : 1996-07-12

Application Number : 20630

Regulatory Info : RX

Registration Country : USA

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20

Iran Expo
Not Confirmed
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Iran Expo
Not Confirmed

REMIFENTANIL HYDROCHLORIDE

Brand Name : ULTIVA

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 5MG BASE/VIAL

Packaging :

Approval Date : 1996-07-12

Application Number : 20630

Regulatory Info : RX

Registration Country : USA

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