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List of All Manufacturers & Suppliers of Dobutamine HCl Licensing, EU CTD Dossiers, Marketing Authorizations, Finished Dosage Formulations listed on PharmaCompass.com

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01 1Dr. Reddy\'s Laboratories

02 2Naprod Life Sciences

03 2Actavis Inc

04 5Baxter Healthcare Corporation

05 1Bio Labs

06 1Bioindustria L.I.M. Spa

07 1Biotech Laboratories Pty Ltd

08 1Brooks laboratories Limited

09 2Cooper Pharma Limited

10 1Eli Lilly

11 4Farbe Firma

12 1Fisiopharma S.r.l.

13 1Flagship Biotech International Pvt. Ltd

14 2Fresenius SE & Co. KGaA

15 1Ha Noi CPC1 Pharmaceutical JSC

16 2Hainan Poly Pharm

17 2Hameln Pharma GmbH

18 1Harson Laboratories

19 2Hikma Pharmaceuticals

20 10Hospira, Inc.

21 1Igenius Life Sciences

22 1Infugen Pharma

23 1Lifespan Biotech

24 1Luitpold Pharmaceuticals, Inc.

25 1Micro Healthcare

26 1Myungmoon Pharm. Co., LTD.

27 1Polifarma

28 1RANBAXY LABORATORIES LIMITED

29 2Sandoz B2B

30 1Slate Run Pharmaceuticals

31 1Teligent, Inc

32 1Teva Pharmaceutical Industries

33 1Verve Human Care Laboratories

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PharmaCompass

01

  • 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

DOBUTAMINE HYDROCHLORIDE

Brand Name : DOBUTAMINE HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 12.5MG BASE/ML

Packaging :

Approval Date : 1998-03-31

Application Number : 74995

Regulatory Info : DISCN

Registration Country : USA

Dr Reddy Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothNaprod is a top player in Oncology & Anesthesia FDF through excellent innovation, discovery of new processes & high-quality production.

Regulatory Info :

Registration Country : India

Dobutamine Hydrochloride

Brand Name :

Dosage Form : Lyophilised Injection

Dosage Strength : 250MG/Vial

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Naprod Life Sciences

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothNaprod is a top player in Oncology & Anesthesia FDF through excellent innovation, discovery of new processes & high-quality production.

Regulatory Info :

Registration Country : India

Dobutamine Hydrochloride

Brand Name :

Dosage Form : Liquid Injection

Dosage Strength : 250MG/20ML

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Naprod Life Sciences

04

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DOBUTAMINE HYDROCHLORIDE

Brand Name : DOBUTAMINE HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 12.5MG BASE/ML

Packaging :

Approval Date : 1993-11-30

Application Number : 74114

Regulatory Info : DISCN

Registration Country : USA

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DOBUTAMINE HYDROCHLORIDE

Brand Name : DOBUTAMINE HYDROCHLORIDE IN DEXTROSE 5% IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 50MG BASE/100ML

Packaging :

Approval Date : 1993-10-19

Application Number : 20255

Regulatory Info : RX

Registration Country : USA

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DOBUTAMINE HYDROCHLORIDE

Brand Name : DOBUTAMINE HYDROCHLORIDE IN DEXTROSE 5% IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 100MG BASE/100ML

Packaging :

Approval Date : 1993-10-19

Application Number : 20255

Regulatory Info : RX

Registration Country : USA

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DOBUTAMINE HYDROCHLORIDE

Brand Name : DOBUTAMINE HYDROCHLORIDE IN DEXTROSE 5% IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 200MG BASE/100ML

Packaging :

Approval Date : 1993-10-19

Application Number : 20255

Regulatory Info : RX

Registration Country : USA

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DOBUTAMINE HYDROCHLORIDE

Brand Name : DOBUTAMINE HYDROCHLORIDE IN DEXTROSE 5% IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 400MG BASE/100ML

Packaging :

Approval Date : 1993-10-19

Application Number : 20255

Regulatory Info : RX

Registration Country : USA

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DOBUTAMINE HYDROCHLORIDE

Brand Name : DOBUTREX

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 12.5MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1982-01-01

Application Number : 17820

Regulatory Info : DISCN

Registration Country : USA

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DOBUTAMINE HYDROCHLORIDE

Brand Name : DOBUTAMINE HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 12.5MG BASE/ML

Packaging :

Approval Date : 1994-10-31

Application Number : 74277

Regulatory Info : RX

Registration Country : USA

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DOBUTAMINE HYDROCHLORIDE

Brand Name : DOBUTAMINE HYDROCHLORIDE IN DEXTROSE 5% IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 200MG BASE/100ML

Packaging :

Approval Date : 1993-10-19

Application Number : 20201

Regulatory Info : RX

Registration Country : USA

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DOBUTAMINE HYDROCHLORIDE

Brand Name : DOBUTAMINE HYDROCHLORIDE IN DEXTROSE 5% IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 100MG BASE/100ML

Packaging :

Approval Date : 1993-10-19

Application Number : 20201

Regulatory Info : RX

Registration Country : USA

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DOBUTAMINE HYDROCHLORIDE

Brand Name : DOBUTAMINE HYDROCHLORIDE IN DEXTROSE 5% IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 50MG BASE/100ML

Packaging :

Approval Date : 1993-10-19

Application Number : 20201

Regulatory Info : RX

Registration Country : USA

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DOBUTAMINE HYDROCHLORIDE

Brand Name : DOBUTAMINE HYDROCHLORIDE IN DEXTROSE 5% IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 400MG BASE/100ML

Packaging :

Approval Date : 1994-07-07

Application Number : 20201

Regulatory Info : RX

Registration Country : USA

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DOBUTAMINE HYDROCHLORIDE

Brand Name : DOBUTAMINE HYDROCHLORIDE IN DEXTROSE 5%

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 50MG BASE/100ML

Packaging :

Approval Date : 1993-10-19

Application Number : 20269

Regulatory Info : DISCN

Registration Country : USA

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DOBUTAMINE HYDROCHLORIDE

Brand Name : DOBUTAMINE HYDROCHLORIDE IN DEXTROSE 5%

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 100MG BASE/100ML

Packaging :

Approval Date : 1993-10-19

Application Number : 20269

Regulatory Info : DISCN

Registration Country : USA

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DOBUTAMINE HYDROCHLORIDE

Brand Name : DOBUTAMINE HYDROCHLORIDE IN DEXTROSE 5%

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 200MG BASE/100ML

Packaging :

Approval Date : 1993-10-19

Application Number : 20269

Regulatory Info : DISCN

Registration Country : USA

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DOBUTAMINE HYDROCHLORIDE

Brand Name : DOBUTAMINE HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 12.5MG BASE/ML

Packaging :

Approval Date : 1993-11-29

Application Number : 74086

Regulatory Info : RX

Registration Country : USA

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DOBUTAMINE HYDROCHLORIDE

Brand Name : DOBUTAMINE HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 12.5MG BASE/ML

Packaging :

Approval Date : 1995-02-21

Application Number : 74098

Regulatory Info : DISCN

Registration Country : USA

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DOBUTAMINE HYDROCHLORIDE

Brand Name : DOBUTAMINE HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 12.5MG BASE/ML

Packaging :

Approval Date : 1993-10-19

Application Number : 74206

Regulatory Info : DISCN

Registration Country : USA

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