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01 1Sanofi

02 2Mankind Pharma

03 1Activo Health

04 1Adcock Ingram

05 3Aguettant

06 1Auro Pharma Inc

07 2Aurobindo Pharma Limited

08 1B. Braun Medical

09 3B. Braun Melsungen AG

10 1Bharat Parenterals Limited

11 1Biotech Laboratories Pty Ltd

12 2Caplin Point Laboratories Limited

13 1Cipla Medpro South Africa

14 1Cristalia Produtos Quimicos Farma. Ltda

15 1Eugia Pharma

16 4Farbe Firma

17 1Flagship Biotech International Pvt. Ltd

18 3Fresenius Kabi AB Brunna

19 2Fresenius Kabi AG

20 4Fresenius Kabi USA

21 2Fresenius SE & Co. KGaA

22 2GLAND PHARMA LIMITED

23 1Hameln Pharma GmbH

24 1Hanlim Pharmaceuticals Inc

25 1Health Biotech

26 3Hikma Pharmaceuticals

27 2Hospira, Inc.

28 1JAMP PHARMA

29 2Juno Pharmaceuticals Pty Ltd

30 1Kalcex

31 1Labatec Pharm

32 2Lunan Pharmaceutical

33 1MS Pharma

34 2MSD Pharmaceuticals

35 1Macleods Pharmaceuticals Limited

36 1Maiva Pharma

37 2Meitheal Pharmaceuticals

38 6Merck & Co

39 2Myungmoon Pharm. Co., LTD.

40 1Naprod Life Sciences

41 1Noridem Enterprises Limited

42 1Noridem Enterprises Ltd

43 5ORIFARM GROUP AS

44 2Organon

45 1Pfizer Inc

46 1Pharma Dynamics

47 2Pharmachim Ab

48 2Piramal Enterprises Limited

49 2Pluviaendo

50 2Polifarma

51 2Prinston

52 1Rajasthan Antibiotics

53 2Rising Pharmaceuticals Inc

54 2Sagent Pharmaceuticals

55 3Sandoz B2B

56 1Schering Plough Sa

57 1Steriscience

58 3Tamarang

59 2Teva Pharmaceutical Industries

60 2Themis Medicare

61 3Viatris

62 2West-ward Pharmaceutical Corp

63 2Zhejiang Xianju Pharmaceutical Co. Ltd

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info : Originator

Registration Country : South Africa

Rocuronium bromide

Brand Name : Esmeron

Dosage Form : INJ

Dosage Strength : 50mg/5ml

Packaging : 5X10mg/5ml

Approval Date :

Application Number :

Regulatory Info : Originator

Registration Country : South Africa

Sanofi Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDelivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.

Regulatory Info : RX

Registration Country : USA

ROCURONIUM BROMIDE

Brand Name : ROCURONIUM BROMIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 50MG/5ML (10MG/ML)

Packaging :

Approval Date : 2025-05-29

Application Number : 219674

Regulatory Info : RX

Registration Country : USA

Company Banner

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDelivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.

Regulatory Info : RX

Registration Country : USA

ROCURONIUM BROMIDE

Brand Name : ROCURONIUM BROMIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 100MG/10ML (10MG/ML)

Packaging :

Approval Date : 2025-05-29

Application Number : 219674

Regulatory Info : RX

Registration Country : USA

Company Banner

04

CTAD25
Not Confirmed
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CTAD25
Not Confirmed

ROCURONIUM BROMIDE

Brand Name : ROCURONIUM BROMIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 50MG/5ML (10MG/ML)

Packaging :

Approval Date : 2008-12-29

Application Number : 78651

Regulatory Info : RX

Registration Country : USA

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05

CTAD25
Not Confirmed
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CTAD25
Not Confirmed

ROCURONIUM BROMIDE

Brand Name : ROCURONIUM BROMIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 100MG/10ML (10MG/ML)

Packaging :

Approval Date : 2008-12-29

Application Number : 78651

Regulatory Info : RX

Registration Country : USA

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06

CTAD25
Not Confirmed
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CTAD25
Not Confirmed

ROCURONIUM BROMIDE

Brand Name : ROCURONIUM BROMIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 50MG/5ML (10MG/ML)

Packaging :

Approval Date : 2008-11-26

Application Number : 78519

Regulatory Info : RX

Registration Country : USA

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07

CTAD25
Not Confirmed
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CTAD25
Not Confirmed

ROCURONIUM BROMIDE

Brand Name : ROCURONIUM BROMIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 100MG/10ML (10MG/ML)

Packaging :

Approval Date : 2008-11-26

Application Number : 78519

Regulatory Info : RX

Registration Country : USA

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08

CTAD25
Not Confirmed
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CTAD25
Not Confirmed

ROCURONIUM BROMIDE

Brand Name : ZEMURON

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 50MG/5ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1994-03-17

Application Number : 20214

Regulatory Info : DISCN

Registration Country : USA

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09

CTAD25
Not Confirmed
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CTAD25
Not Confirmed

ROCURONIUM BROMIDE

Brand Name : ZEMURON

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 10MG/ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1994-03-17

Application Number : 20214

Regulatory Info : DISCN

Registration Country : USA

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10

CTAD25
Not Confirmed
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CTAD25
Not Confirmed

ROCURONIUM BROMIDE

Brand Name : ZEMURON

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 100MG/10ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1994-03-17

Application Number : 20214

Regulatory Info : DISCN

Registration Country : USA

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11

CTAD25
Not Confirmed
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CTAD25
Not Confirmed

ROCURONIUM BROMIDE

Brand Name : ROCURONIUM BROMIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 50MG/5ML (10MG/ML)

Packaging :

Approval Date : 2010-07-28

Application Number : 91458

Regulatory Info : RX

Registration Country : USA

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12

CTAD25
Not Confirmed
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CTAD25
Not Confirmed

ROCURONIUM BROMIDE

Brand Name : ROCURONIUM BROMIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 100MG/10ML (10MG/ML)

Packaging :

Approval Date : 2010-07-28

Application Number : 91458

Regulatory Info : RX

Registration Country : USA

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13

CTAD25
Not Confirmed
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CTAD25
Not Confirmed

ROCURONIUM BROMIDE

Brand Name : ROCURONIUM BROMIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 50MG/5ML (10MG/ML)

Packaging :

Approval Date : 2008-12-05

Application Number : 79195

Regulatory Info : RX

Registration Country : USA

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14

CTAD25
Not Confirmed
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CTAD25
Not Confirmed

ROCURONIUM BROMIDE

Brand Name : ROCURONIUM BROMIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 100MG/10ML (10MG/ML)

Packaging :

Approval Date : 2008-12-05

Application Number : 79195

Regulatory Info : RX

Registration Country : USA

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15

CTAD25
Not Confirmed
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CTAD25
Not Confirmed

ROCURONIUM BROMIDE

Brand Name : ROCURONIUM BROMIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 50MG/5ML (10MG/ML)

Packaging :

Approval Date : 2012-08-27

Application Number : 91115

Regulatory Info : RX

Registration Country : USA

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16

CTAD25
Not Confirmed
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CTAD25
Not Confirmed

ROCURONIUM BROMIDE

Brand Name : ROCURONIUM BROMIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 100MG/10ML (10MG/ML)

Packaging :

Approval Date : 2012-08-27

Application Number : 91115

Regulatory Info : RX

Registration Country : USA

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17

CTAD25
Not Confirmed
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CTAD25
Not Confirmed

ROCURONIUM BROMIDE

Brand Name : ROCURONIUM BROMIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 50MG/5ML (10MG/ML)

Packaging :

Approval Date : 2008-11-26

Application Number : 78717

Regulatory Info : DISCN

Registration Country : USA

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18

CTAD25
Not Confirmed
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CTAD25
Not Confirmed

ROCURONIUM BROMIDE

Brand Name : ROCURONIUM BROMIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 100MG/10ML (10MG/ML)

Packaging :

Approval Date : 2008-11-26

Application Number : 78717

Regulatory Info : DISCN

Registration Country : USA

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19

CTAD25
Not Confirmed
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CTAD25
Not Confirmed

ROCURONIUM BROMIDE

Brand Name : ROCURONIUM BROMIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 50MG/5ML (10MG/ML)

Packaging :

Approval Date : 2008-11-26

Application Number : 79199

Regulatory Info : RX

Registration Country : USA

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20

CTAD25
Not Confirmed
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CTAD25
Not Confirmed

ROCURONIUM BROMIDE

Brand Name : ROCURONIUM BROMIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 100MG/10ML (10MG/ML)

Packaging :

Approval Date : 2008-11-26

Application Number : 79199

Regulatory Info : RX

Registration Country : USA

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