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01 4Sanofi

02 1Dr. Reddy's Laboratories

03 2ANI Pharmaceuticals Inc

04 1Adcock Ingram

05 1Areva Pharmaceuticals

06 1AstraZeneca

07 1Chartwell Pharmaceuticals llc

08 1Epic Pharma. LLC.

09 1Fresenius Kabi USA

10 1Ha Noi CPC1 Pharmaceutical JSC

11 1Hikma Pharmaceuticals

12 2Impax Laboratories

13 2Lannett Company, Inc.

14 1Novartis Pharmaceuticals Corporation

15 1Pharmacare Premium

16 2TWi Pharmaceuticals

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PharmaCompass

01

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BioAsia
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

Regulatory Info : DISCN

Registration Country : USA

TERBUTALINE SULFATE

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

Sanofi Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

Regulatory Info : DISCN

Registration Country : USA

TERBUTALINE SULFATE

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

Dr Reddy Company Banner

03

arrow
BioAsia
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

Regulatory Info : DISCN

Registration Country : USA

TERBUTALINE SULFATE

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 Company Banner

04

arrow
BioAsia
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

Regulatory Info : DISCN

Registration Country : USA

TERBUTALINE SULFATE

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 Company Banner

05

arrow
BioAsia
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

Regulatory Info : DISCN

Registration Country : USA

TERBUTALINE SULFATE

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

Sanofi Company Banner

06

The Generic Rx Session
Not Confirmed
arrow
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The Generic Rx Session
Not Confirmed

Terbutaline Sulfate

Brand Name : Bronchoped

Dosage Form : SYR

Dosage Strength : 25mg/5ml

Packaging : 100X1mg/5ml

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : South Africa

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07

BioAsia
Not Confirmed
arrow
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BioAsia
Not Confirmed

TERBUTALINE SULFATE

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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08

BioAsia
Not Confirmed
arrow
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BioAsia
Not Confirmed

TERBUTALINE SULFATE

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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09

BioAsia
Not Confirmed
arrow
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BioAsia
Not Confirmed

TERBUTALINE SULFATE

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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10

BioAsia
Not Confirmed
arrow
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BioAsia
Not Confirmed

TERBUTALINE SULFATE

Brand Name : BRICANYL TURBUHALER

Dosage Form : POWDER

Dosage Strength : 0.5MG/DOSE

Packaging :

Approval Date :

Application Number : 786616

Regulatory Info :

Registration Country : Canada

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11

BioAsia
Not Confirmed
arrow
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BioAsia
Not Confirmed

TERBUTALINE SULFATE

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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12

The Generic Rx Session
Not Confirmed
arrow
arrow
The Generic Rx Session
Not Confirmed

TERBUTALINE SULFATE

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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13

BioAsia
Not Confirmed
arrow
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BioAsia
Not Confirmed

TERBUTALINE SULFATE

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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14

The Generic Rx Session
Not Confirmed
arrow
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The Generic Rx Session
Not Confirmed

Terbutaline Sulfate; Guaifenesin

Brand Name : Guacanyl

Dosage Form : Oral Solution

Dosage Strength : 1.5MG/5ML; 66.5MG/5ML

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Vietnam

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15

BioAsia
Not Confirmed
arrow
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BioAsia
Not Confirmed

TERBUTALINE SULFATE

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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16

BioAsia
Not Confirmed
arrow
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BioAsia
Not Confirmed

TERBUTALINE SULFATE

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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17

The Generic Rx Session
Not Confirmed
arrow
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The Generic Rx Session
Not Confirmed

TERBUTALINE SULFATE

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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18

The Generic Rx Session
Not Confirmed
arrow
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The Generic Rx Session
Not Confirmed

TERBUTALINE SULFATE

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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19

The Generic Rx Session
Not Confirmed
arrow
arrow
The Generic Rx Session
Not Confirmed

TERBUTALINE SULFATE

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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20

The Generic Rx Session
Not Confirmed
arrow
arrow
The Generic Rx Session
Not Confirmed

TERBUTALINE SULFATE

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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21

BioAsia
Not Confirmed
arrow
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BioAsia
Not Confirmed

TERBUTALINE SULFATE

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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22

BioAsia
Not Confirmed
arrow
arrow
BioAsia
Not Confirmed

TERBUTALINE SULFATE

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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23

BioAsia
Not Confirmed
arrow
arrow
BioAsia
Not Confirmed

TERBUTALINE SULFATE

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

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