01 1ANIDRO DO BRASIL EXTRACOES S.A. Parnaíba BR
02 1SOURCETECH QUIMICA LTDA. Pindamonhangaba BR
03 1SPERA NEXUS, INC. Shizuoka JP
04 1ZHEJIANG AUSUN PHARMACEUTICAL CO., LTD. Taizhou CN
01 4Pilocarpine hydrochloride
01 2Brazil
02 1China
03 1Japan
01 4Valid
Certificate Number : R1-CEP 1999-005 - Rev 03
Status : Valid
Issue Date : 2021-10-25
Type : Chemical
Substance Number : 633
Certificate Number : R1-CEP 1997-034 - Rev 05
Status : Valid
Issue Date : 2023-06-08
Type : Chemical
Substance Number : 633
Certificate Number : CEP 2015-343 - Rev 02
Status : Valid
Issue Date : 2024-04-29
Type : Chemical
Substance Number : 633
Certificate Number : CEP 2023-367 - Rev 00
Status : Valid
Issue Date : 2025-04-02
Type : Chemical
Substance Number : 633
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PharmaCompass offers a list of Pilocarpine Hydrochloride 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 Pilocarpine Hydrochloride manufacturer or Pilocarpine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pilocarpine Hydrochloride manufacturer or Pilocarpine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Pilocarpine Hydrochloride API Price utilized in the formulation of products. Pilocarpine Hydrochloride API Price is not always fixed or binding as the Pilocarpine Hydrochloride Price is obtained through a variety of data sources. The Pilocarpine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 54-71-7 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 54-71-7, including repackagers and relabelers. The FDA regulates 54-71-7 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 54-71-7 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 54-71-7 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 54-71-7 supplier is an individual or a company that provides 54-71-7 active pharmaceutical ingredient (API) or 54-71-7 finished formulations upon request. The 54-71-7 suppliers may include 54-71-7 API manufacturers, exporters, distributors and traders.
click here to find a list of 54-71-7 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A 54-71-7 CEP of the European Pharmacopoeia monograph is often referred to as a 54-71-7 Certificate of Suitability (COS). The purpose of a 54-71-7 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of 54-71-7 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of 54-71-7 to their clients by showing that a 54-71-7 CEP has been issued for it. The manufacturer submits a 54-71-7 CEP (COS) as part of the market authorization procedure, and it takes on the role of a 54-71-7 CEP holder for the record. Additionally, the data presented in the 54-71-7 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the 54-71-7 DMF.
A 54-71-7 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. 54-71-7 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 54-71-7 suppliers with CEP (COS) on PharmaCompass.
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