Aspen API. More than just an API™
01 3Aspen API
02 11Aspen Pharmacare Holdings
03 6Orion Corporation
04 3Accord healthcare
05 3Adcock Ingram
06 6B. Braun Medical
07 3B. Braun Melsungen AG
08 3Bioglan
09 4Cristalia Produtos Quimicos Farma. Ltda
10 2Farmatek
11 4Fresenius Kabi AB Brunna
12 3Fresenius Kabi AG
13 3Fresenius Kabi USA
14 4GSK
15 6Hameln Pharma GmbH
16 3Hanlim Pharmaceuticals Inc
17 3Hikma Pharmaceuticals
18 3Hospira Uk Limited
19 3Hospira, Inc.
20 3Karo Pharma
21 3Kern Pharma S.L.
22 3LABORATORIOS NORMON SA
23 3Leman Skl Sa
24 3Nivagen
25 3Noridem Enterprises Limited
26 3Pfizer Inc
27 3Pharma Dynamics
28 3Reig Jofre
29 2STERIMAX INC
30 3Sandoz B2B
31 3Teva Pharmaceutical Industries
32 2Themis Medicare
33 9Viatris
34 3Yichang Humanwell Pharmaceutical
01 21INJ
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 25Generic
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 1REMIFENTANIL 1 mg ADCO
08 1REMIFENTANIL 2 mg ADCO
09 1REMIFENTANIL 5 mg ADCO
10 13REMIFENTANIL HYDROCHLORIDE
11 2REMIFENTANIL HYDROCHLORIDE FOR INJECTION
12 1REMITHEM 1 mg Vial
13 1REMITHEM 2 mg Vial
14 2Remifentanil 1 mg B. Braun
15 1Remifentanil 1mg Viatris
16 2Remifentanil 2 mg B. Braun
17 1Remifentanil 2mg Viatris
18 2Remifentanil 5 mg B. Braun
19 1Remifentanil 5mg Viatris
20 3Remifentanil Actavis
21 3Remifentanil B. Braun
22 3Remifentanil Fresenius
23 3Remifentanil Fresenius Kabi
24 3Remifentanil Hameln
25 6Remifentanil Hospira
26 3Remifentanil Kern Pharma
27 3Remifentanil Leman IV
28 3Remifentanil Mylan
29 3Remifentanil Noridem
30 3Remifentanil Normon
31 6Remifentanil Orion
32 3Remifentanil Pfizer
33 3Remifentanil Reig Jofre
34 3Remifentanil Sandoz
35 3Remifentanil Teva
36 3Remifentanil hameln
37 3Remifentanilo Accord
38 1Remifentanilo Kabi
39 3Remifentanilo Sala
40 3ULTIAN
41 3ULTIVA
42 12Ultiva
43 1Ultiva 1 mg
44 1Ultiva 2 mg
45 1Ultiva 5 Injection
46 5Blank
01 4Brazil
02 2Canada
03 3China
04 2India
05 9Norway
06 21South 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
