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01 2Macfarlan Smith Limited
02 1Saneca Pharmaceuticals as
03 1Yichang Humanwell Pharmaceutical Co., Ltd.
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01 1Baeksu Pharmaceutical Co., Ltd.
02 1Nosa Chemical Co., Ltd.
03 2Samung Industrial Co., Ltd.
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01 4Fentanyl citrate
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01 1China
02 1Slovakia
03 2U.S.A
Registrant Name : Baeksu Pharmaceutical Co., Ltd.
Registration Date : 2021-06-22
Registration Number : 20210622-210-J-918
Manufacturer Name : Macfarlan Smith Limited
Manufacturer Address : 10 Wheatfield Road, Edinburgh, EH11 2QA, United Kingdom
Registrant Name : Samung Industrial Co., Ltd.
Registration Date : 2021-06-22
Registration Number : 20210622-210-J-918(A)
Manufacturer Name : Macfarlan Smith Limited
Manufacturer Address : 10 Wheatfield Road, Edinburgh, EH11 2QA, United Kingdom
Registrant Name : Nosa Chemical Co., Ltd.
Registration Date : 2021-04-05
Registration Number : 20210405-210-J-919
Manufacturer Name : Saneca Pharmaceuticals as
Manufacturer Address : Nitrianska 100, 920 27 Hlohovec, Slovak Republic
Registrant Name : Samung Industrial Co., Ltd.
Registration Date : 2022-02-15
Registration Number : 20220215-210-J-1232
Manufacturer Name : Yichang Humanwell Pharmaceut...
Manufacturer Address : No.19, Dalian Road, Yichang Development Zone, Hubei, China
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PharmaCompass offers a list of Fentanyl Citrate 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 Fentanyl Citrate manufacturer or Fentanyl Citrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Fentanyl Citrate manufacturer or Fentanyl Citrate supplier.
PharmaCompass also assists you with knowing the Fentanyl Citrate API Price utilized in the formulation of products. Fentanyl Citrate API Price is not always fixed or binding as the Fentanyl Citrate Price is obtained through a variety of data sources. The Fentanyl Citrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A LAZANDA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LAZANDA, including repackagers and relabelers. The FDA regulates LAZANDA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LAZANDA 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 LAZANDA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A LAZANDA supplier is an individual or a company that provides LAZANDA active pharmaceutical ingredient (API) or LAZANDA finished formulations upon request. The LAZANDA suppliers may include LAZANDA API manufacturers, exporters, distributors and traders.
click here to find a list of LAZANDA suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a LAZANDA Drug Master File in Korea (LAZANDA KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of LAZANDA. The MFDS reviews the LAZANDA KDMF as part of the drug registration process and uses the information provided in the LAZANDA KDMF to evaluate the safety and efficacy of the drug.
After submitting a LAZANDA KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their LAZANDA API can apply through the Korea Drug Master File (KDMF).
click here to find a list of LAZANDA suppliers with KDMF on PharmaCompass.
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