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 12care4
04 2ANI Pharmaceuticals Inc
05 1Adcock Ingram
06 1Areva Pharmaceuticals
07 22AstraZeneca
08 1Chartwell Pharmaceuticals llc
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01 2AEROSOL, METERED;INHALATION
02 8INJECTABLE;INJECTION
03 36Inhalation Powder
04 2Inhalation Solution
05 3Inhalation Spray
06 3Oral Solution
07 1POWDER
08 2Powder For Inhalation
09 1SYR
10 1Solution
11 1Solution For Inhalation
12 4Solution For Injection
13 10TABLET;ORAL
14 7Tablet
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01 1Allowed
02 6Approved
03 3Authorized
04 9DISCN
05 38Deregistered
06 1Generic
07 4Marketed
08 6Not Marketed
09 1Prescription
10 11RX
11 1Blank
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01 1BRETHAIRE
02 3BRETHINE
03 4BRICANYL
04 1BRICANYL TURBUHALER
05 13Bricanyl
06 5Bricanyl Depot
07 35Bricanyl Turbuhaler
08 1Bronchoped
09 1Dracanyl Turbuhaler
10 1Earth Basmin
11 1Guacanyl
12 12TERBUTALINE SULFATE
13 1Terbasmin Expectorante
14 2Terbasmin Turbuhaler
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01 1Canada
02 10Norway
03 1South Africa
04 3Spain
05 44Sweden
06 1Switzerland
07 20USA
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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
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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

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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

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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

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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

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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

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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

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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

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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

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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

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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

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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

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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

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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

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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

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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
