01 1NEWCHEM SPA
02 2STERLING SPA
01 3NOMEGESTROL ACETATE
01 3Italy
NDC Package Code : 24002-0013
Start Marketing Date : 2009-08-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 64918-1002
Start Marketing Date : 2011-11-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 64918-1004
Start Marketing Date : 2020-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Nomegestrol Acetate 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 Nomegestrol Acetate manufacturer or Nomegestrol Acetate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Nomegestrol Acetate manufacturer or Nomegestrol Acetate supplier.
PharmaCompass also assists you with knowing the Nomegestrol Acetate API Price utilized in the formulation of products. Nomegestrol Acetate API Price is not always fixed or binding as the Nomegestrol Acetate Price is obtained through a variety of data sources. The Nomegestrol Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lutenyl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lutenyl, including repackagers and relabelers. The FDA regulates Lutenyl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lutenyl 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 Lutenyl manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lutenyl supplier is an individual or a company that provides Lutenyl active pharmaceutical ingredient (API) or Lutenyl finished formulations upon request. The Lutenyl suppliers may include Lutenyl API manufacturers, exporters, distributors and traders.
click here to find a list of Lutenyl suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Lutenyl as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Lutenyl API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Lutenyl as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Lutenyl and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Lutenyl NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Lutenyl suppliers with NDC on PharmaCompass.
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