Axplora is your partner of choice for complex APIs.
01 1FARMABIOS S.p.A Gropello Cairoli IT
02 1Pharmacia & Upjohn Company Kalamazoo US
03 1SYMBIOTEC PHARMALAB LIMITED Indore IN
01 1Methylprednisolone acetate
02 1Methylprednisolone acetate, Micronised
03 1Methylprednisolone acetate, Micronised, Sterile
01 1Italy
02 1U.S.A
03 1Blank
01 2Valid
02 1Withdrawn by Holder
Axplora is your partner of choice for complex APIs.
Axplora is your partner of choice for complex APIs.
Methylprednisolone Acetate, Micronised, Sterile
Certificate Number : R0-CEP 2021-429 - Rev 00
Status : Valid
Issue Date : 2023-06-23
Type : Chemical
Substance Number : 933
Certificate Number : R0-CEP 2000-363 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2001-10-24
Type : TSE
Substance Number : 933
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Methylprednisolone Acetate, Micronised
Certificate Number : CEP 2011-063 - Rev 02
Status : Valid
Issue Date : 2026-04-02
Type : Chemical
Substance Number : 933
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PharmaCompass offers a list of Methylprednisolone Acetate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Methylprednisolone Acetate manufacturer or Methylprednisolone Acetate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Methylprednisolone Acetate manufacturer or Methylprednisolone Acetate supplier.
A Methylprednisolone Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Methylprednisolone Acetate, including repackagers and relabelers. The FDA regulates Methylprednisolone Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Methylprednisolone Acetate 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 Methylprednisolone Acetate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Methylprednisolone Acetate supplier is an individual or a company that provides Methylprednisolone Acetate active pharmaceutical ingredient (API) or Methylprednisolone Acetate finished formulations upon request. The Methylprednisolone Acetate suppliers may include Methylprednisolone Acetate API manufacturers, exporters, distributors and traders.
click here to find a list of Methylprednisolone Acetate suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Methylprednisolone Acetate CEP of the European Pharmacopoeia monograph is often referred to as a Methylprednisolone Acetate Certificate of Suitability (COS). The purpose of a Methylprednisolone Acetate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Methylprednisolone Acetate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Methylprednisolone Acetate to their clients by showing that a Methylprednisolone Acetate CEP has been issued for it. The manufacturer submits a Methylprednisolone Acetate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Methylprednisolone Acetate CEP holder for the record. Additionally, the data presented in the Methylprednisolone Acetate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Methylprednisolone Acetate DMF.
A Methylprednisolone Acetate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Methylprednisolone Acetate 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 Methylprednisolone Acetate suppliers with CEP (COS) on PharmaCompass.
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