Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
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01 2Sanofi
02 2Actavis Inc
03 2Aurobindo Pharma Limited
04 2Cooper Pharma Limited
05 2Cristalia Produtos Quimicos Farma. Ltda
06 1Demo S.A.
07 2Flagship Biotech International Pvt. Ltd
08 2GLAND PHARMA LIMITED
09 6Hikma Pharmaceuticals
10 3Hospira, Inc.
11 2Meitheal Pharmaceuticals
12 3Merck & Co
13 2Myungmoon Pharm. Co., LTD.
14 2Naprod Life Sciences
15 1ORIFARM GROUP AS
16 1Omnia L?kemedel Ab
17 1Organon
18 2Osper Formulations
19 1Polifarma
20 2Rajasthan Antibiotics
21 2Sagent Pharmaceuticals
22 4Sun Pharmaceutical Industries Limited
23 2Themis Medicare
24 2Viatris
25 1Yangtze River Pharmaceutical Group
26 1Zhejiang Xianju Pharmaceutical Co. Ltd
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01 5INJ
02 25INJECTABLE;INJECTION
03 4INJECTION
04 9Injection
05 1LYOPHILIZED POWDER FOR SOLUTION FOR INJECTION
06 4Lyophilised Injection
07 1Lyophilized powder for injection
08 2Powder For Solution For Injection
09 1Powder for injection fluid, resolution
10 1Powder to Prepare Injection Solution
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01 7DISCN
02 2Deregistered
03 9Generic
04 3Originator
05 18RX
06 14Blank
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01 2Muscuron
02 2NORCURON
03 5Norcuron
04 1Norcuron 10mg
05 2VECURON
06 23VECURONIUM BROMIDE
07 2Vecron
08 1Zyvec 10
09 1Zyvec 4
10 14Blank
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01 2Brazil
02 2China
03 12India
04 1Norway
05 5South Africa
06 2South Korea
07 2Sweden
08 1Turkey
09 25USA
10 1Blank
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Norcuron
Dosage Form : INJ
Dosage Strength : 4mg
Packaging : 10X1mg
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Norcuron
Dosage Form : INJ
Dosage Strength : 4mg
Packaging : 50X1mg
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
Regulatory Info : DISCN
Registration Country : USA
Brand Name : VECURONIUM BROMIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 10MG/VIAL
Packaging :
Approval Date : 1995-08-31
Application Number : 74334
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : VECURONIUM BROMIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 20MG/VIAL
Packaging :
Approval Date : 1995-08-31
Application Number : 74334
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : VECURONIUM BROMIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 10MG/VIAL
Packaging :
Approval Date : 1999-08-23
Application Number : 75218
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : VECURONIUM BROMIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 20MG/VIAL
Packaging :
Approval Date : 1999-08-23
Application Number : 75218
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : VECURONIUM BROMIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 10MG/VIAL
Packaging :
Approval Date : 2000-06-13
Application Number : 75549
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : VECURONIUM BROMIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 20MG/VIAL
Packaging :
Approval Date : 2000-06-13
Application Number : 75549
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : VECURONIUM BROMIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 10MG/VIAL
Packaging :
Approval Date : 1999-10-21
Application Number : 75164
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : VECURONIUM BROMIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 20MG/VIAL
Packaging :
Approval Date : 1999-10-21
Application Number : 75164
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : VECURONIUM BROMIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 4MG/VIAL
Packaging :
Approval Date : 2001-09-11
Application Number : 75558
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : VECURONIUM BROMIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 10MG/VIAL
Packaging :
Approval Date : 1999-08-25
Application Number : 74688
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : VECURONIUM BROMIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 20MG/VIAL
Packaging :
Approval Date : 1999-08-25
Application Number : 74688
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NORCURON
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 10MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1984-04-30
Application Number : 18776
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NORCURON
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 20MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1992-01-03
Application Number : 18776
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : VECURONIUM BROMIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 10MG/VIAL
Packaging :
Approval Date : 2008-12-29
Application Number : 78274
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : VECURONIUM BROMIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 20MG/VIAL
Packaging :
Approval Date : 2008-12-29
Application Number : 78274
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : VECURONIUM BROMIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 10MG/VIAL
Packaging :
Approval Date : 2009-06-17
Application Number : 79001
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : VECURONIUM BROMIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 20MG/VIAL
Packaging :
Approval Date : 2009-06-17
Application Number : 79001
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : VECURONIUM BROMIDE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 10MG/VIAL
Packaging :
Approval Date : 2010-05-11
Application Number : 90243
Regulatory Info : RX
Registration Country : USA