Veranova: A CDMO that manages complexity with confidence.
01 1Veranova, L.P.
02 1LSNE, Inc
03 1MSN Life Sciences Private Limited
04 1Patheon Italia S.p.A.
01 1CANGRELOR
02 2Cangrelor
03 1Cangrelor Tetra Sodium
01 1India
02 3U.S.A
NDC Package Code : 50137-3312
Start Marketing Date : 2015-06-22
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 69766-060
Start Marketing Date : 2018-11-29
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 68225-062
Start Marketing Date : 2015-07-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION (50mg/1)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 73301-003
Start Marketing Date : 2015-07-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
A Cangrelor manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cangrelor, including repackagers and relabelers. The FDA regulates Cangrelor manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cangrelor 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 Cangrelor manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cangrelor supplier is an individual or a company that provides Cangrelor active pharmaceutical ingredient (API) or Cangrelor finished formulations upon request. The Cangrelor suppliers may include Cangrelor API manufacturers, exporters, distributors and traders.
click here to find a list of Cangrelor 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 Cangrelor as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Cangrelor 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 Cangrelor 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 Cangrelor and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Cangrelor NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Cangrelor suppliers with NDC on PharmaCompass.
We have 4 companies offering Cangrelor
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