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PharmaCompass offers a list of Levonorgestrel 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 Levonorgestrel manufacturer or Levonorgestrel supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Levonorgestrel manufacturer or Levonorgestrel supplier.
PharmaCompass also assists you with knowing the Levonorgestrel API Price utilized in the formulation of products. Levonorgestrel API Price is not always fixed or binding as the Levonorgestrel Price is obtained through a variety of data sources. The Levonorgestrel Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A (+-)-Norgestrel manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of (+-)-Norgestrel, including repackagers and relabelers. The FDA regulates (+-)-Norgestrel manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. (+-)-Norgestrel 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 (+-)-Norgestrel manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A (+-)-Norgestrel supplier is an individual or a company that provides (+-)-Norgestrel active pharmaceutical ingredient (API) or (+-)-Norgestrel finished formulations upon request. The (+-)-Norgestrel suppliers may include (+-)-Norgestrel API manufacturers, exporters, distributors and traders.
click here to find a list of (+-)-Norgestrel suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A (+-)-Norgestrel CEP of the European Pharmacopoeia monograph is often referred to as a (+-)-Norgestrel Certificate of Suitability (COS). The purpose of a (+-)-Norgestrel CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of (+-)-Norgestrel EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of (+-)-Norgestrel to their clients by showing that a (+-)-Norgestrel CEP has been issued for it. The manufacturer submits a (+-)-Norgestrel CEP (COS) as part of the market authorization procedure, and it takes on the role of a (+-)-Norgestrel CEP holder for the record. Additionally, the data presented in the (+-)-Norgestrel CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the (+-)-Norgestrel DMF.
A (+-)-Norgestrel CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. (+-)-Norgestrel 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 (+-)-Norgestrel suppliers with CEP (COS) on PharmaCompass.
We have 8 companies offering (+-)-Norgestrel
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