ASolution Pharmaceuticals: Your CDMO Partner for APIs and Specialty Molecules.
01 1ASOLUTION PHARMACEUTICALS PVT. LTD. Thane IN
02 2MAITHRI DRUGS PRIVATE LIMITED Bonthapally Village IN
03 2ALEMBIC PHARMACEUTICALS LIMITED Vadodara IN
04 2F.I.S. - FABBRICA ITALIANA SINTETICI S.P.A. Montecchio Maggiore IT
05 1JINAN JINDA PHARMACEUTICAL CHEMISTRY CO., LTD. Zhangqiu CN
06 1MACLEODS PHARMACEUTICALS LIMITED Mumbai IN
07 2MANGALAM DRUGS & ORGANICS LTD. Mumbai IN
08 1MYLAN LABORATORIES LIMITED Hyderabad IN
09 1OMSAV PHARMA RESEARCH PRIVATE LIMITED Mumbai IN
ASolution Pharmaceuticals: Your CDMO Partner for APIs and Specialty Molecules.
Certificate Number : CEP 2023-346 - Rev 00
Status : Valid
Issue Date : 2025-06-19
Type : Chemical
Substance Number : 101
Maithri Drugs: Dedicated to your API needs.
Certificate Number : R0-CEP 2022-074 - Rev 00
Status : Valid
Issue Date : 2022-12-12
Type : Chemical
Substance Number : 101
Maithri Drugs: Dedicated to your API needs.
Certificate Number : CEP 2019-262 - Rev 01
Status : Valid
Issue Date : 2024-05-02
Type : Chemical
Substance Number : 101
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PharmaCompass offers a list of Nitrofurantoin 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 Nitrofurantoin manufacturer or Nitrofurantoin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Nitrofurantoin manufacturer or Nitrofurantoin supplier.
PharmaCompass also assists you with knowing the Nitrofurantoin API Price utilized in the formulation of products. Nitrofurantoin API Price is not always fixed or binding as the Nitrofurantoin Price is obtained through a variety of data sources. The Nitrofurantoin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A N0883 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of N0883, including repackagers and relabelers. The FDA regulates N0883 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. N0883 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 N0883 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A N0883 supplier is an individual or a company that provides N0883 active pharmaceutical ingredient (API) or N0883 finished formulations upon request. The N0883 suppliers may include N0883 API manufacturers, exporters, distributors and traders.
click here to find a list of N0883 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A N0883 CEP of the European Pharmacopoeia monograph is often referred to as a N0883 Certificate of Suitability (COS). The purpose of a N0883 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of N0883 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of N0883 to their clients by showing that a N0883 CEP has been issued for it. The manufacturer submits a N0883 CEP (COS) as part of the market authorization procedure, and it takes on the role of a N0883 CEP holder for the record. Additionally, the data presented in the N0883 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the N0883 DMF.
A N0883 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. N0883 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 N0883 suppliers with CEP (COS) on PharmaCompass.
We have 9 companies offering N0883
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