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

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01 1Sanofi
02 5Dr. Reddy's Laboratories
03 1Polfa Tarchomin
04 1NanoAlvand
05 2Supriya Lifescience
06 4Ever Pharma
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01 1Fulvestrant 250Mg 5Ml 1 Units Parenteral Use
02 1Fulvestrant 250Mg 5Ml 2 Units Parenteral Use
03 3INJ
04 1INJECTION
05 4Injectable Solution
06 14Injectable Solution In Pre-Filled Syringe
07 9Injection
08 1Injection
09 2Injection fluid, resolution
10 1Liquid Injection
11 5PFS
12 1Pre Filled Syringes
13 1Pre-Filled Syringe
14 1Prefilled Syringe
15 6SOLUTION
16 19SOLUTION;INTRAMUSCULAR
17 23Solution For Injection
18 1Solution for Injection
19 1Solution for Injection in Pre-Filled Syringe
20 5Blank
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01 7Allowed
02 12Approved
03 1Authorised
04 15Authorized
05 4DISCN
06 1Deregistered
07 1Dossier Availability: Q1 2027
08 8Generic
09 1Lead Market Dossiers- Approved in both US & EU
10 1Lead Market Dossiers- Filed
11 1Originator
12 6Prescription
13 15RX
14 1Suspensed
15 1Withdrawn
16 25Blank
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01 2Ambiful
02 1Eranfu 250
03 3FASLODEX
04 1FASTELEV
05 1FULVEKAST
06 1FULVESER
07 17FULVESTRANT
08 1FULVESTRANT ACCORD
09 1FULVESTRANT EVER PHARMA
10 1FULVESTRANT INJECTABLE
11 3FULVESTRANT INJECTION
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13 1FULVETHER
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51 1TEVA-FULVESTRANT INJECTION
52 1VESTRANT
53 10Blank
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01 5Australia
02 1Austria
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07 2Italy
08 2Malta
09 3Moldova
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11 1Poland
12 1Saudi Arabia
13 8South Africa
14 16Spain
15 13Sweden
16 7Switzerland
17 19USA
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : Allowed
Registration Country : Switzerland
Brand Name : Fulvestrant Zentiva
Dosage Form : Solution For Injection
Dosage Strength : 250mg/5ml
Packaging :
Approval Date : 24/05/2021
Application Number : 68281
Regulatory Info : Allowed
Registration Country : Switzerland
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : RX
Registration Country : USA
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
Polfa 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
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
Regulatory Info :
Registration Country : Iran
Brand Name : Fularent
Dosage Form : Prefilled Syringe
Dosage Strength : 250MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Iran
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Injection
Dosage Strength : 250MG/5ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Ever Pharma, highly specialized CDMO in producing complex injectables including high potency & controlled substances, suspensions, etc.
Regulatory Info :
Registration Country : Austria
Brand Name : Fulvestrant
Dosage Form : Solution for Injection in Pre-Filled Syringe
Dosage Strength : 250MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Austria
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : Lead Market Dossiers- Filed
Registration Country : India
Brand Name :
Dosage Form : Injection
Dosage Strength : 50MG/ML
Packaging :
Approval Date :
Application Number :
Regulatory Info : Lead Market Dossiers- Filed
Registration Country : India
DRL 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
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
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Fulvestrant Reddy
Dosage Form : Solution For Injection
Dosage Strength : 250mg
Packaging :
Approval Date : 28/07/2022
Application Number : 20200917000016
Regulatory Info : Approved
Registration Country : Sweden
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : Generic
Registration Country : South Africa
Brand Name : Eranfu 250
Dosage Form : PFS
Dosage Strength : 250mg/5ml
Packaging : 5X2mg/5ml
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Injection
Dosage Strength : 50MG/ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Ever Pharma, highly specialized CDMO in producing complex injectables including high potency & controlled substances, suspensions, etc.
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Fulvestrant Ever Pharma
Dosage Form : Solution For Injection
Dosage Strength : 250mg
Packaging :
Approval Date : 17/09/2020
Application Number : 20200226000011
Regulatory Info : Approved
Registration Country : Sweden
Ever Pharma, highly specialized CDMO in producing complex injectables including high potency & controlled substances, suspensions, etc.
Regulatory Info : Authorized
Registration Country : Spain
Brand Name : Ambiful
Dosage Form : Injectable Solution In Pre-Filled Syringe
Dosage Strength : 250MG
Packaging :
Approval Date : 2019-07-11
Application Number : 83793
Regulatory Info : Authorized
Registration Country : Spain
Ever Pharma, highly specialized CDMO in producing complex injectables including high potency & controlled substances, suspensions, etc.
Regulatory Info : Authorised
Registration Country : Malta
Brand Name : Fulvestrant Ever Valinject
Dosage Form : Solution For Injection
Dosage Strength : 250ML/5ML
Packaging :
Approval Date : 2022-05-03
Application Number :
Regulatory Info : Authorised
Registration Country : Malta
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Regulatory Info : RX
Registration Country : USA
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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Regulatory Info : DISCN
Registration Country : USA
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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Regulatory Info : DISCN
Registration Country : USA
Brand Name : FULVESTRANT
Dosage Form : SOLUTION;INTRAMUSCULAR
Dosage Strength : 250MG/5ML (50MG/ML)
Packaging :
Approval Date : 2019-07-23
Application Number : 208811
Regulatory Info : DISCN
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
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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Regulatory Info : RX
Registration Country : USA
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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Regulatory Info : RX
Registration Country : USA
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
