Aspen API. More than just an API™
01 3Aspen API
02 11Aspen Pharmacare Holdings
03 6Orion Corporation
04 3Accord healthcare
05 6B. Braun Medical
06 3B. Braun Melsungen AG
07 3Bioglan
08 4Cristalia Produtos Quimicos Farma. Ltda
09 2Farmatek
10 4Fresenius Kabi AB Brunna
11 3Fresenius Kabi AG
12 3Fresenius Kabi USA
13 4GSK
14 6Hameln Pharma GmbH
15 3Hanlim Pharmaceuticals Inc
16 3Hikma Pharmaceuticals
17 3Hospira Uk Limited
18 3Hospira, Inc.
19 3Karo Pharma
20 3Kern Pharma S.L.
21 3LABORATORIOS NORMON SA
22 3Leman Skl Sa
23 3Nivagen
24 3Noridem Enterprises Limited
25 3Pfizer Inc
26 3Pharma Dynamics
27 3Reig Jofre
28 2STERIMAX INC
29 3Sandoz B2B
30 3Teva Pharmaceutical Industries
31 2Themis Medicare
32 6Viatris
33 3Viatris South Africa (Pty) Ltd
34 3Yichang Humanwell Pharmaceutical
01 18INJ
02 12INJECTABLE;INJECTION
03 7INJECTION
04 5Injection
05 39Injection/Infusion Solution
06 2Lyophilized Powder
07 2POWDER FOR SOLUTION
08 13Powder For Concentrate For Injection And Infusion Solution
09 6Powder For Concentrate For Injection Or Infusion Solution
10 6Powder For Concentrate For Solution For Infusion
11 3Powder for concentrate for injection/infusion solution, solution
12 3Powder for injection/infusion fluid, resolution
13 3Powder to concentrate to the Injection/infusion fluid, resolution
14 3Solution For Injection
01 9Allowed
02 15Approved
03 15Authorized
04 4Cancelled
05 24Deregistered
06 22Generic
07 2NARCOTICS (CDSA I)
08 3Originator
09 12RX
10 16Blank
01 1Altirem IV 1 mg
02 1Altirem IV 2 mg
03 1Altirem IV 5 mg
04 1Fortiva 1mg
05 1Fortiva 2mg
06 1Fortiva 5mg
07 13REMIFENTANIL HYDROCHLORIDE
08 2REMIFENTANIL HYDROCHLORIDE FOR INJECTION
09 1REMITHEM 1 mg Vial
10 1REMITHEM 2 mg Vial
11 2Remifentanil 1 mg B. Braun
12 1Remifentanil 1mg Viatris
13 2Remifentanil 2 mg B. Braun
14 1Remifentanil 2mg Viatris
15 2Remifentanil 5 mg B. Braun
16 1Remifentanil 5mg Viatris
17 3Remifentanil Actavis
18 3Remifentanil B. Braun
19 3Remifentanil Fresenius
20 3Remifentanil Fresenius Kabi
21 3Remifentanil Hameln
22 6Remifentanil Hospira
23 3Remifentanil Kern Pharma
24 3Remifentanil Leman IV
25 3Remifentanil Mylan
26 3Remifentanil Noridem
27 3Remifentanil Normon
28 6Remifentanil Orion
29 3Remifentanil Pfizer
30 3Remifentanil Reig Jofre
31 3Remifentanil Sandoz
32 3Remifentanil Teva
33 3Remifentanil hameln
34 3Remifentanilo Accord
35 1Remifentanilo Kabi
36 3Remifentanilo Sala
37 3ULTIAN
38 3ULTIVA
39 12Ultiva
40 1Ultiva 1 mg
41 1Ultiva 2 mg
42 1Ultiva 5 Injection
43 5Blank
01 4Brazil
02 2Canada
03 3China
04 2India
05 9Norway
06 18South Africa
07 3South Korea
08 19Spain
09 39Sweden
10 9Switzerland
11 2Turkey
12 12USA
Aspen API. More than just an API™
Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Ultiva
Dosage Form : Powder For Concentrate For Injection And Infusion Solution
Dosage Strength : 1MG
Packaging :
Approval Date : 1997-07-01
Application Number : 61488
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Ultiva
Dosage Form : Powder For Concentrate For Solution For Infusion
Dosage Strength : 1mg
Packaging :
Approval Date : 20/11/1996
Application Number : 53747
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Remifentanil Orion
Dosage Form : Injection/Infusion Solution
Dosage Strength :
Packaging :
Approval Date : 24/07/2023
Application Number : 20220429000168
Regulatory Info : Approved
Registration Country : Sweden
Aspen API. More than just an API™
Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Ultiva
Dosage Form : Powder For Concentrate For Injection And Infusion Solution
Dosage Strength : 5MG
Packaging :
Approval Date : 1997-07-01
Application Number : 61490
Regulatory Info : Authorized
Registration Country : Spain
Aspen API. More than just an API™
Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Ultiva
Dosage Form : Powder For Concentrate For Injection And Infusion Solution
Dosage Strength : 2MG
Packaging :
Approval Date : 1997-07-01
Application Number : 61489
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Ultiva
Dosage Form : Powder For Concentrate For Solution For Infusion
Dosage Strength : 2mg
Packaging :
Approval Date : 20/11/1996
Application Number : 53747
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Ultiva
Dosage Form : Powder For Concentrate For Solution For Infusion
Dosage Strength : 5mg
Packaging :
Approval Date : 20/11/1996
Application Number : 53747
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Ultiva
Dosage Form : Injection/Infusion Solution
Dosage Strength :
Packaging :
Approval Date : 06/02/1998
Application Number : 19980206000074
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Ultiva
Dosage Form : Injection/Infusion Solution
Dosage Strength : 2mg
Packaging :
Approval Date : 06/02/1998
Application Number : 19980206000081
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Ultiva
Dosage Form : Injection/Infusion Solution
Dosage Strength : 5mg
Packaging :
Approval Date : 06/02/1998
Application Number : 19980206000098
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Generic
Registration Country : South Africa
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
Regulatory Info : Generic
Registration Country : South Africa
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
Regulatory Info : Generic
Registration Country : South Africa
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
Regulatory Info : Originator
Registration Country : South Africa
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
Regulatory Info : Originator
Registration Country : South Africa
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
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Remifentanil Orion
Dosage Form : Injection/Infusion Solution
Dosage Strength : 2mg
Packaging :
Approval Date : 24/07/2023
Application Number : 20220429000175
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Remifentanil Orion
Dosage Form : Injection/Infusion Solution
Dosage Strength : 5mg
Packaging :
Approval Date : 24/07/2023
Application Number : 20220429000182
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Brand Name : Remifentanil Orion
Dosage Form : Injection/Infusion Solution
Dosage Strength :
Packaging :
Approval Date : 16/12/2010
Application Number : 20090609000024
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Brand Name : Remifentanil Orion
Dosage Form : Injection/Infusion Solution
Dosage Strength : 2mg
Packaging :
Approval Date : 16/12/2010
Application Number : 20090609000031
Regulatory Info : Deregistered
Registration Country : Sweden
Regulatory Info : Deregistered
Registration Country : Sweden
Brand Name : Remifentanil Orion
Dosage Form : Injection/Infusion Solution
Dosage Strength : 5mg
Packaging :
Approval Date : 16/12/2010
Application Number : 20090609000048
Regulatory Info : Deregistered
Registration Country : Sweden
