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Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions. 
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01 Seqens (1)
02 Axplora (1)
03 GLAND PHARMA LIMITED (1)
04 Hangzhou Jiuyuan Gene Engineering (1)
05 Hansoh Pharma (1)
06 Industriale Chimica s.r.l. (1)
07 Lianyungang Runzhong Pharmaceutical Co Ltd (1)
08 ScinoPharm Taiwan, Ltd (1)
09 Sinopep Pharmaceutical Inc (2)
10 Sterling Spa (1)
11 Steroid SpA (1)
12 Teva API (2)
13 Wisdom Pharmaceutical Co., Ltd. (1)
01 FULVESTRANT (8)
02 FULVESTRANT INTERMEDIATE (1)
03 FULVESTRANT INTERMEDIATE (CAS NO.: 875573-66-3) (1)
04 FULVESTRANT USP (3)
05 FULVESTRANT USP, NON-STERILE BULK DRUG SUBSTANCE (1)
06 FULVESTRANT, NON-STERILE, BULK DRUG SUBSTANCE (1)
01 China (6)
02 France (1)
03 Germany (1)
04 India (1)
05 Israel (2)
06 Italy (3)
07 Taiwan (1)
01 Active (14)
02 Inactive (1)
01 Complete (11)
02 Blank (4)
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PharmaCompass offers a list of Fulvestrant API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Fulvestrant manufacturer or Fulvestrant supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Fulvestrant manufacturer or Fulvestrant supplier.
PharmaCompass also assists you with knowing the Fulvestrant API Price utilized in the formulation of products. Fulvestrant API Price is not always fixed or binding as the Fulvestrant Price is obtained through a variety of data sources. The Fulvestrant Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A NCGC00024964-02 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of NCGC00024964-02, including repackagers and relabelers. The FDA regulates NCGC00024964-02 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. NCGC00024964-02 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of NCGC00024964-02 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A NCGC00024964-02 supplier is an individual or a company that provides NCGC00024964-02 active pharmaceutical ingredient (API) or NCGC00024964-02 finished formulations upon request. The NCGC00024964-02 suppliers may include NCGC00024964-02 API manufacturers, exporters, distributors and traders.
click here to find a list of NCGC00024964-02 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A NCGC00024964-02 DMF (Drug Master File) is a document detailing the whole manufacturing process of NCGC00024964-02 active pharmaceutical ingredient (API) in detail. Different forms of NCGC00024964-02 DMFs exist exist since differing nations have different regulations, such as NCGC00024964-02 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A NCGC00024964-02 DMF submitted to regulatory agencies in the US is known as a USDMF. NCGC00024964-02 USDMF includes data on NCGC00024964-02's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The NCGC00024964-02 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of NCGC00024964-02 suppliers with USDMF on PharmaCompass.
We have 13 companies offering NCGC00024964-02
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