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01 3AbbVie Inc
02 2Aspen API
03 6Aspen Pharmacare Holdings
04 2Pharmathen SA
05 8Accord healthcare
06 2Aurobindo Pharma Limited
07 1Bharat Parenterals Limited
08 2Caplin Point Laboratories Limited
09 4Cristalia Produtos Quimicos Farma. Ltda
10 8Farbe Firma
11 1Fresenius Kabi AB Brunna
12 3Fresenius Kabi USA
13 1Fresenius SE & Co. KGaA
14 3GLAND PHARMA LIMITED
15 4GSK
16 3Hainan Poly Pharm
17 5Health Biotech
18 4Hikma Pharmaceuticals
19 3Hospira, Inc.
20 5Jiangsu Hengrui Medicine
21 1Kalcex
22 2LABORATORIOS NORMON SA
23 1MS Pharma
24 3Meitheal Pharmaceuticals
25 2Montage Laboratories
26 2Naprod Life Sciences
27 1Omega Laboratories Limited
28 1Pfizer Inc
29 2Piramal Pharma Solutions
30 1Pluviaendo
31 3Rajasthan Antibiotics
32 2Reig Jofre
33 3Safeline Pharmaceuticals
34 3Sagent Pharmaceuticals
35 3Sandoz B2B
36 3Somerset Pharmaceuticals Inc
37 2Themis Medicare
38 3Viatris
39 1Zhejiang Xianju Pharmaceutical Co. Ltd
40 3Zydus Pharmaceuticals
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01 1Ampoule
02 3INF
03 8INJ
04 46INJECTABLE;INJECTION
05 4INJECTION
06 10Injectable And Infusion Solution
07 2Injectable Solution
08 2Injectable Solution/Infusion
09 11Injection
10 1Injection
11 2Injection fluid, resolution
12 7Liquid Injection
13 1Lyophilized powder for injection
14 1SOLUTION
15 1SOLUTION
16 4Solution For Injection
17 3Solution For Injection/Infusion
18 5Vial
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01 2Allowed
02 9Authorized
03 3Cancelled
04 14DISCN
05 5Deregistered
06 2EU Approved
07 8Generic
08 1Generic CTD- Available
09 7Originator
10 1Prescription
11 31RX
12 1US ANDA- Submitted
13 28Blank
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01 4CIS
02 1CISATRACURIUM 10mg/5ml FRESENIUS
03 30CISATRACURIUM BESYLATE
04 1CISATRACURIUM BESYLATE INJECTION USP MULTIDOSE
05 13CISATRACURIUM BESYLATE PRESERVATIVE FREE
06 1CISATRACURIUM SAFELINE 10 mg
07 1CISATRACURIUM SAFELINE 20 mg
08 1CISATRACURIUM SAFELINE 5 MG
09 2Cisatra
10 1Cisatracurio Hikma
11 1Cisatracurio Kabi
12 1Cisatracurio Kalceks
13 1Cisatracurio Pfizer
14 2Cisatracurium Accordpharma
15 2Cisatracurium Besylate
16 3Cisatracurium Mylan
17 2Cisatracurium Normon
18 2Cisatracurius Hall
19 1Cistrax 10 mg/ 5 ml
20 1Cistrax 150 mg/30 ml
21 1Cistrax 5 mg/2,5 ml
22 1NIMBEX
23 2NIMBEX PRESERVATIVE FREE
24 7Nimbex
25 1Nimbex
26 1Nimbex 2 mg/ml (10 ml)
27 1Nimbex 2 mg/ml (2,5 ml)
28 1Nimbex 2 mg/ml (5 ml)
29 1Nimbex 5
30 25Blank
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01 4Brazil
02 1Canada
03 2China
04 2Greece
05 23India
06 1Jordan
07 2Norway
08 11South Africa
09 12Spain
10 5Sweden
11 2Switzerland
12 1Turkey
13 46USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NIMBEX
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 2MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1995-12-15
Application Number : 20551
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Nimbex
Dosage Form : Injectable Solution/Infusion
Dosage Strength : 5MG
Packaging :
Approval Date : 2002-09-11
Application Number : 61199
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Nimbex
Dosage Form : Solution For Injection
Dosage Strength : 5mg/2.5ml
Packaging :
Approval Date : 15/01/1997
Application Number : 53677
Regulatory Info : Allowed
Registration Country : Switzerland
Pharmathen provides life cycle Management solutions for branded pharma, as well as to develop & establish new technology platforms.
Regulatory Info : EU Approved
Registration Country : Greece
Brand Name :
Dosage Form : Solution For Injection
Dosage Strength : 2MG/ML
Packaging :
Approval Date :
Application Number :
Regulatory Info : EU Approved
Registration Country : Greece
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NIMBEX PRESERVATIVE FREE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 10MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1995-12-15
Application Number : 20551
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NIMBEX PRESERVATIVE FREE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 2MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1995-12-15
Application Number : 20551
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : Cancelled
Registration Country : Spain
Brand Name : Nimbex
Dosage Form : Injectable Solution/Infusion
Dosage Strength : 2MG
Packaging :
Approval Date : 1996-11-01
Application Number : 61200
Regulatory Info : Cancelled
Registration Country : Spain
Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Nimbex
Dosage Form : Solution For Injection
Dosage Strength : 20mg/10ml
Packaging :
Approval Date : 15/01/1997
Application Number : 53677
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Nimbex 2 mg/ml (2,5 ml)
Dosage Form : INJ
Dosage Strength : 2mg/ml
Packaging : 2.5X5mg/ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Nimbex 2 mg/ml (5 ml)
Dosage Form : INJ
Dosage Strength : 2mg/ml
Packaging : 5X5mg/ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Nimbex 2 mg/ml (10 ml)
Dosage Form : INJ
Dosage Strength : 2mg/ml
Packaging : 10X5mg/ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Nimbex 5
Dosage Form : INJ
Dosage Strength : 5mg/ml
Packaging : 30X1mg/ml
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Pharmathen provides life cycle Management solutions for branded pharma, as well as to develop & establish new technology platforms.
Regulatory Info : EU Approved
Registration Country : Greece
Brand Name :
Dosage Form : Solution For Injection
Dosage Strength : 5MG/ML
Packaging :
Approval Date :
Application Number :
Regulatory Info : EU Approved
Registration Country : Greece
Regulatory Info : RX
Registration Country : USA
Brand Name : CISATRACURIUM BESYLATE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 2MG BASE/ML
Packaging :
Approval Date : 2022-06-28
Application Number : 203078
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : CISATRACURIUM BESYLATE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 2MG BASE/ML
Packaging :
Approval Date : 2020-11-06
Application Number : 201836
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : CISATRACURIUM BESYLATE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 10MG BASE/ML
Packaging :
Approval Date : 2020-11-06
Application Number : 201836
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : CISATRACURIUM BESYLATE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 2MG BASE/ML
Packaging :
Approval Date : 2020-11-06
Application Number : 201851
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : CISATRACURIUM BESYLATE PRESERVATIVE FREE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 2MG BASE/ML
Packaging :
Approval Date : 2012-02-03
Application Number : 200154
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : CISATRACURIUM BESYLATE PRESERVATIVE FREE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 10MG BASE/ML
Packaging :
Approval Date : 2012-02-03
Application Number : 200154
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : CISATRACURIUM BESYLATE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 2MG BASE/ML
Packaging :
Approval Date : 2012-02-03
Application Number : 200159
Regulatory Info : RX
Registration Country : USA