Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
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01 4Sanofi
02 1Dr. Reddy's Laboratories
03 2ANI Pharmaceuticals Inc
04 1Adcock Ingram
05 1Areva Pharmaceuticals
06 13AstraZeneca
07 1Chartwell Pharmaceuticals llc
08 2Ecowest Ab
09 1Epic Pharma. LLC.
10 1Fresenius Kabi USA
11 1Ha Noi CPC1 Pharmaceutical JSC
12 1Hikma Pharmaceuticals
13 2Impax Laboratories
14 1Laboratorios ERN
15 1Lailan Sa Laboratory
16 2Lannett Company, Inc.
17 1Medartuum
18 1Novartis Pharmaceuticals Corporation
19 9ORIFARM GROUP AS
20 1Parallel Pharma Ab
21 6Paranova Pharmaceuticals Ab
22 1Pharmacare Premium
23 4Pharmachim Ab
24 2Pharmel Ab
25 2TWi Pharmaceuticals
26 5Teva Pharmaceutical Industries
27 3Unimedic AB
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01 2AEROSOL, METERED;INHALATION
02 8INJECTABLE;INJECTION
03 31Inhalation Powder
04 2Inhalation Solution
05 3Inhalation Spray
06 3Oral Solution
07 1POWDER
08 2Powder For Inhalation
09 1SYR
10 1Solution For Injection
11 10TABLET;ORAL
12 6Tablet
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01 1Allowed
02 6Approved
03 2Authorized
04 9DISCN
05 38Deregistered
06 1Generic
07 1Prescription
08 11RX
09 1Blank
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01 1BRETHAIRE
02 3BRETHINE
03 4BRICANYL
04 1BRICANYL TURBUHALER
05 9Bricanyl
06 4Bricanyl Depot
07 30Bricanyl Turbuhaler
08 1Bronchoped
09 1Dracanyl Turbuhaler
10 1Earth Basmin
11 1Guacanyl
12 12TERBUTALINE SULFATE
13 2Terbasmin Turbuhaler
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01 1Canada
02 1South Africa
03 2Spain
04 44Sweden
05 1Switzerland
06 20USA
07 1Vietnam
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BRICANYL
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 1MG/ML
Packaging :
Approval Date : 1982-01-01
Application Number : 17466
Regulatory Info : DISCN
Registration Country : USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : DISCN
Registration Country : USA
Brand Name : TERBUTALINE SULFATE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 1MG/ML
Packaging :
Approval Date : 2004-07-20
Application Number : 76853
Regulatory Info : DISCN
Registration Country : USA
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BRICANYL
Dosage Form : TABLET;ORAL
Dosage Strength : 2.5MG
Packaging :
Approval Date : 1982-01-01
Application Number : 17618
Regulatory Info : DISCN
Registration Country : USA
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BRICANYL
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Packaging :
Approval Date : 1982-01-01
Application Number : 17618
Regulatory Info : DISCN
Registration Country : USA
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BRICANYL
Dosage Form : AEROSOL, METERED;INHALATION
Dosage Strength : 0.2MG/INH
Packaging :
Approval Date : 1985-03-19
Application Number : 18000
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : BRETHINE
Dosage Form : TABLET;ORAL
Dosage Strength : 2.5MG
Packaging :
Approval Date : 1982-01-01
Application Number : 17849
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : BRETHINE
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Packaging :
Approval Date : 1982-01-01
Application Number : 17849
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : TERBUTALINE SULFATE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 1MG/ML
Packaging :
Approval Date : 2013-11-08
Application Number : 200122
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : TERBUTALINE SULFATE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 1MG/ML
Packaging :
Approval Date : 2004-04-23
Application Number : 76770
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : TERBUTALINE SULFATE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 1MG/ML
Packaging :
Approval Date : 2008-01-07
Application Number : 78151
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : TERBUTALINE SULFATE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 1MG/ML
Packaging :
Approval Date : 2004-05-26
Application Number : 76887
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : TERBUTALINE SULFATE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 1MG/ML
Packaging :
Approval Date : 2009-05-20
Application Number : 78630
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : TERBUTALINE SULFATE
Dosage Form : TABLET;ORAL
Dosage Strength : 2.5MG
Packaging :
Approval Date : 2001-06-26
Application Number : 75877
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : TERBUTALINE SULFATE
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Packaging :
Approval Date : 2001-06-26
Application Number : 75877
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : TERBUTALINE SULFATE
Dosage Form : TABLET;ORAL
Dosage Strength : 2.5MG
Packaging :
Approval Date : 2005-03-25
Application Number : 77152
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : TERBUTALINE SULFATE
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Packaging :
Approval Date : 2005-03-25
Application Number : 77152
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BRETHAIRE
Dosage Form : AEROSOL, METERED;INHALATION
Dosage Strength : 0.2MG/INH
Packaging :
Approval Date : 1984-08-17
Application Number : 18762
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BRETHINE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 1MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 18571
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : TERBUTALINE SULFATE
Dosage Form : TABLET;ORAL
Dosage Strength : 2.5MG
Packaging :
Approval Date : 2020-06-19
Application Number : 211832
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : TERBUTALINE SULFATE
Dosage Form : TABLET;ORAL
Dosage Strength : 5MG
Packaging :
Approval Date : 2020-06-19
Application Number : 211832
Regulatory Info : RX
Registration Country : USA