Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
01 1SYMBIOTEC PHARMALAB PRIVATE LIMITED Indore IN
02 1Farmabios SpA Gropello Cairoli IT
03 1CURIA SPAIN S.A.U. Boecillo ES
04 1HENAN LIHUA PHARMACEUTICAL CO., LTD. Anyang CN
05 1SYMBIOTICA SPECIALITY INGREDIENTS SDN. BHD. Butterworth MY
06 1TARO PHARMACEUTICAL INDUSTRIES, LTD. Haifa Bay IL
07 1TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL
08 1TIANJIN TIANYAO PHARMACEUTICALS CO., LTD. Tianjin CN
Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
Betamethasone Dipropionate, Micronised
Certificate Number : R1-CEP 2012-079 - Rev 00
Status : Valid
Issue Date : 2018-02-19
Type : Chemical
Substance Number : 809
Axplora is your partner of choice for complex APIs.
Betamethasone Dipropionate, Micronised
Certificate Number : R1-CEP 2003-232 - Rev 03
Status : Valid
Issue Date : 2023-02-08
Type : Chemical
Substance Number : 809
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PharmaCompass offers a list of Betamethasone Dipropionate 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 Betamethasone Dipropionate manufacturer or Betamethasone Dipropionate supplier for your needs.
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PharmaCompass also assists you with knowing the Betamethasone Dipropionate API Price utilized in the formulation of products. Betamethasone Dipropionate API Price is not always fixed or binding as the Betamethasone Dipropionate Price is obtained through a variety of data sources. The Betamethasone Dipropionate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Maxivate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Maxivate, including repackagers and relabelers. The FDA regulates Maxivate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Maxivate 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 Maxivate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Maxivate supplier is an individual or a company that provides Maxivate active pharmaceutical ingredient (API) or Maxivate finished formulations upon request. The Maxivate suppliers may include Maxivate API manufacturers, exporters, distributors and traders.
click here to find a list of Maxivate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Maxivate CEP of the European Pharmacopoeia monograph is often referred to as a Maxivate Certificate of Suitability (COS). The purpose of a Maxivate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Maxivate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Maxivate to their clients by showing that a Maxivate CEP has been issued for it. The manufacturer submits a Maxivate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Maxivate CEP holder for the record. Additionally, the data presented in the Maxivate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Maxivate DMF.
A Maxivate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Maxivate CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Maxivate suppliers with CEP (COS) on PharmaCompass.
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