Farmhispania Group, a leading European CDMO in HPAPI Technologies & High Potency Fermentation.
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01 1Farmhispania, S.A.
02 3Chunghwa Chemical Synthesis & Biotech. Ltd
03 1Chunghwa Chemical Sysnthsis & Biotech Co.,Ltd.
04 3Biocon Limited
05 1Biocon limited
06 1BrightGene Bio-Medical Technology Co., Ltd.
07 1CONCORD BIOTECH LTD
08 1MSN Laboratories Private Limited
09 1NATCO PHARMA LIMITED
10 1Novartis Pharmaceuticals Corporation
11 1ScinoPharm Taiwan Ltd.
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01 2EVEROLIMUS
02 10Everolimus
03 1Everolimus B02
04 1Everolimus Premix 2 %
05 1everolimus
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01 1China
02 7India
03 1Spain
04 1Switzerland
05 5Taiwan
NDC Package Code : 17404-1027
Start Marketing Date : 2019-12-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
NDC Package Code : 52076-6234
Start Marketing Date : 2018-01-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
NDC Package Code : 52076-6247
Start Marketing Date : 2018-01-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
NDC Package Code : 52076-6253
Start Marketing Date : 2018-01-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
NDC Package Code : 52076-6270
Start Marketing Date : 2021-02-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65727-046
Start Marketing Date : 2014-09-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62227-019
Start Marketing Date : 2020-12-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 54893-0126
Start Marketing Date : 2024-03-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 0078-1406
Start Marketing Date : 2009-03-31
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65129-1324
Start Marketing Date : 2015-01-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
19
PharmaCompass offers a list of Everolimus 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 Everolimus manufacturer or Everolimus supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Everolimus manufacturer or Everolimus supplier.
PharmaCompass also assists you with knowing the Everolimus API Price utilized in the formulation of products. Everolimus API Price is not always fixed or binding as the Everolimus Price is obtained through a variety of data sources. The Everolimus Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A RAD manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of RAD, including repackagers and relabelers. The FDA regulates RAD manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. RAD 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 RAD manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A RAD supplier is an individual or a company that provides RAD active pharmaceutical ingredient (API) or RAD finished formulations upon request. The RAD suppliers may include RAD API manufacturers, exporters, distributors and traders.
click here to find a list of RAD 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 RAD as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for RAD 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 RAD 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 RAD and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a RAD NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of RAD suppliers with NDC on PharmaCompass.
We have 9 companies offering RAD
Get in contact with the supplier of your choice: