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Status : Withdrawn by Holder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 Depo-Medrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Depo-Medrate, including repackagers and relabelers. The FDA regulates Depo-Medrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Depo-Medrate 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 Depo-Medrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Depo-Medrate supplier is an individual or a company that provides Depo-Medrate active pharmaceutical ingredient (API) or Depo-Medrate finished formulations upon request. The Depo-Medrate suppliers may include Depo-Medrate API manufacturers, exporters, distributors and traders.
click here to find a list of Depo-Medrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Depo-Medrate CEP of the European Pharmacopoeia monograph is often referred to as a Depo-Medrate Certificate of Suitability (COS). The purpose of a Depo-Medrate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Depo-Medrate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Depo-Medrate to their clients by showing that a Depo-Medrate CEP has been issued for it. The manufacturer submits a Depo-Medrate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Depo-Medrate CEP holder for the record. Additionally, the data presented in the Depo-Medrate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Depo-Medrate DMF.
A Depo-Medrate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Depo-Medrate 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 Depo-Medrate suppliers with CEP (COS) on PharmaCompass.
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