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01 1Sanofi

02 3Dr. Reddy's Laboratories

03 1Polfa Tarchomin

04 1NanoAlvand

05 2Supriya Lifescience

06 1Ever Pharma

07 1AFT Pharmaceuticals

08 4Accord healthcare

09 1Accure Labs

10 1Alembic Pharmaceuticals Limited

11 1Amneal Pharmaceuticals

12 1Apotex Inc

13 12AstraZeneca

14 2Aurobindo Pharma Limited

15 1Avyxa

16 1CHEMO

17 1Chia Tai Tianqing Pharmaceutical Group

18 1Curatis

19 1Dr Reddy's Laboratories (Pty) Ltd

20 1FORMATIVE PHARMA INC.

21 1Fresenius Kabi USA

22 1GetWell Pharmaceutical

23 1Glenmark Pharmaceuticals

24 1HBT Labs

25 1Hangzhou Jiuyuan Gene Engineering

26 1Hansoh Pharma

27 1Intas Pharmaceuticals

28 1InterPharma

29 1JAMP PHARMA

30 1Juno Pharma SA (Pty) Ltd

31 1Sagent Pharmaceuticals

32 1Sakar Healthcare

33 5Sandoz B2B

34 1Swasthya Healthcare

35 3Teva Pharmaceutical Industries

36 1TherDose Pharma

37 2Viatris

38 2Xiromed

39 1Zydus Pharmaceuticals

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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 :

Registration Country : Switzerland

Fulvestrantum

Brand Name : Fulvestrant Zentiva

Dosage Form : Inj Solution

Dosage Strength : 250mg/5ml

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Switzerland

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 : RX

Registration Country : USA

FULVESTRANT

Brand Name : FULVESTRANT

Dosage Form : SOLUTION;INTRAMUSCULAR

Dosage Strength : 250MG/5ML (50MG/ML)

Packaging :

Approval Date : 2020-08-07

Application Number : 209246

Regulatory Info : RX

Registration Country : USA

Dr Reddy Company Banner

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothPolfa Tarchomin is a leading Polish pharmaceutical company with 200 year tradition in manufacture and sale of pharmaceutical products.

Regulatory Info : Dossier Availability: Q1 2027

Registration Country : Poland

Fulvestrant

Brand Name :

Dosage Form : Solution for Injection

Dosage Strength : 250MG/5ML

Packaging :

Approval Date :

Application Number :

Regulatory Info : Dossier Availability: Q1 2027

Registration Country : Poland

Polfa Tarchomin

04

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothNanoAlvand is the entrance to Global Markets as a trusted Highly Potent Products manufacturer.

Regulatory Info :

Registration Country : Iran

Fulvestrant

Brand Name : Fularent

Dosage Form : Prefilled Syringe

Dosage Strength : 250MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Iran

NanoAlvand

05

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSupriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.

Regulatory Info :

Registration Country : India

Fulvestrant

Brand Name :

Dosage Form : Injection

Dosage Strength : 250MG/5ML

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Supriya

06

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothEver Pharma, highly specialized CDMO in producing complex injectables including high potency & controlled substances, suspensions, etc.

Regulatory Info :

Registration Country : Austria

Fulvestrant

Brand Name :

Dosage Form : Solution for Injection in Pre-Filled Syringe

Dosage Strength : 250MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Austria

Ever Pharma CB

07

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info : Lead Market Dossiers- Filed

Registration Country : India

Fulvestrant

Brand Name :

Dosage Form : Injection

Dosage Strength : 50MG/ML

Packaging :

Approval Date :

Application Number :

Regulatory Info : Lead Market Dossiers- Filed

Registration Country : India

Dr Reddy Company Banner

08

  • fda
  • EDQM
  • WHO-GMP

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

Regulatory Info : Lead Market Dossiers- Approved in both US & EU

Registration Country : India

Fulvestrant

Brand Name :

Dosage Form : Injection

Dosage Strength : 250MG/5ML

Packaging :

Approval Date :

Application Number :

Regulatory Info : Lead Market Dossiers- Approved in both US & EU

Registration Country : India

Dr Reddy Company Banner

09

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSupriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.

Regulatory Info :

Registration Country : India

Fulvestrant

Brand Name :

Dosage Form : Injection

Dosage Strength : 50MG/ML

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Supriya

10

Hospitalar
Not Confirmed
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Hospitalar
Not Confirmed

FULVESTRANT

Brand Name : FULVESTRANT

Dosage Form : SOLUTION;INTRAMUSCULAR

Dosage Strength : 250MG/5ML (50MG/ML)

Packaging :

Approval Date : 2019-03-04

Application Number : 210044

Regulatory Info : RX

Registration Country : USA

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11

Hospitalar
Not Confirmed
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Hospitalar
Not Confirmed

FULVESTRANT

Brand Name : FASLODEX

Dosage Form : SOLUTION;INTRAMUSCULAR

Dosage Strength : 250MG/5ML (50MG/ML)

Packaging :

Approval Date : 2002-04-25

Application Number : 21344

Regulatory Info : RX

Registration Country : USA

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12

Hospitalar
Not Confirmed
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Hospitalar
Not Confirmed

FULVESTRANT

Brand Name : FASLODEX

Dosage Form : SOLUTION;INTRAMUSCULAR

Dosage Strength : 125MG/2.5ML (50MG/ML)

Packaging :

Approval Date : 2002-04-25

Application Number : 21344

Regulatory Info : DISCN

Registration Country : USA

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13

Hospitalar
Not Confirmed
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Hospitalar
Not Confirmed

FULVESTRANT

Brand Name : FULVESTRANT

Dosage Form : SOLUTION;INTRAMUSCULAR

Dosage Strength : 250MG/5ML (50MG/ML)

Packaging :

Approval Date : 2019-07-23

Application Number : 208811

Regulatory Info : RX

Registration Country : USA

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14

Hospitalar
Not Confirmed
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Hospitalar
Not Confirmed

FULVESTRANT

Brand Name : FULVESTRANT

Dosage Form : SOLUTION;INTRAMUSCULAR

Dosage Strength : 250MG/5ML (50MG/ML)

Packaging :

Approval Date : 2019-08-19

Application Number : 210063

Regulatory Info : DISCN

Registration Country : USA

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15

Hospitalar
Not Confirmed
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Hospitalar
Not Confirmed

FULVESTRANT

Brand Name : FULVESTRANT

Dosage Form : SOLUTION;INTRAMUSCULAR

Dosage Strength : 250MG/5ML (50MG/ML)

Packaging :

Approval Date : 2020-02-07

Application Number : 211422

Regulatory Info : RX

Registration Country : USA

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16

Hospitalar
Not Confirmed
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Hospitalar
Not Confirmed

FULVESTRANT

Brand Name : FULVESTRANT

Dosage Form : SOLUTION;INTRAMUSCULAR

Dosage Strength : 250MG/5ML (50MG/ML)

Packaging :

Approval Date : 2019-05-20

Application Number : 210326

Regulatory Info : RX

Registration Country : USA

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17

Hospitalar
Not Confirmed
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Hospitalar
Not Confirmed

FULVESTRANT

Brand Name : FULVESTRANT

Dosage Form : SOLUTION;INTRAMUSCULAR

Dosage Strength : 250MG/5ML (50MG/ML)

Packaging :

Approval Date : 2019-08-22

Application Number : 207754

Regulatory Info : RX

Registration Country : USA

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18

Hospitalar
Not Confirmed
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Hospitalar
Not Confirmed

FULVESTRANT

Brand Name : FULVESTRANT

Dosage Form : SOLUTION;INTRAMUSCULAR

Dosage Strength : 250MG/5ML (50MG/ML)

Packaging :

Approval Date : 2019-11-21

Application Number : 209714

Regulatory Info : RX

Registration Country : USA

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19

Hospitalar
Not Confirmed
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Hospitalar
Not Confirmed

FULVESTRANT

Brand Name : FULVESTRANT

Dosage Form : SOLUTION;INTRAMUSCULAR

Dosage Strength : 250MG/5ML (50MG/ML)

Packaging :

Approval Date : 2019-08-22

Application Number : 205871

Regulatory Info : RX

Registration Country : USA

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20

Hospitalar
Not Confirmed
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Hospitalar
Not Confirmed

FULVESTRANT

Brand Name : FULVESTRANT

Dosage Form : SOLUTION;INTRAMUSCULAR

Dosage Strength : 250MG/5ML (50MG/ML)

Packaging :

Approval Date : 2019-05-14

Application Number : 205935

Regulatory Info : RX

Registration Country : USA

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