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01 1R L FINE CHEM PVT. LTD. Bengaluru IN
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01 1Orphenadrine citrate
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01 1India
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01 1Valid
Certificate Number : CEP 2022-094 - Rev 00
Status : Valid
Issue Date : 2024-05-21
Type : Chemical
Substance Number : 1759
57
PharmaCompass offers a list of Orphenadrine 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 Orphenadrine manufacturer or Orphenadrine supplier for your needs.
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PharmaCompass also assists you with knowing the Orphenadrine API Price utilized in the formulation of products. Orphenadrine API Price is not always fixed or binding as the Orphenadrine Price is obtained through a variety of data sources. The Orphenadrine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Flexor manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Flexor, including repackagers and relabelers. The FDA regulates Flexor manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Flexor 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 Flexor manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Flexor supplier is an individual or a company that provides Flexor active pharmaceutical ingredient (API) or Flexor finished formulations upon request. The Flexor suppliers may include Flexor API manufacturers, exporters, distributors and traders.
click here to find a list of Flexor suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Flexor CEP of the European Pharmacopoeia monograph is often referred to as a Flexor Certificate of Suitability (COS). The purpose of a Flexor CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Flexor EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Flexor to their clients by showing that a Flexor CEP has been issued for it. The manufacturer submits a Flexor CEP (COS) as part of the market authorization procedure, and it takes on the role of a Flexor CEP holder for the record. Additionally, the data presented in the Flexor CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Flexor DMF.
A Flexor CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Flexor 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 Flexor suppliers with CEP (COS) on PharmaCompass.