Veranova: A CDMO that manages complexity with confidence.
01 2Macfarlan Smith Limited
02 1SpecGx LLC
01 1Baeksu Pharmaceutical Co., Ltd.
02 1Nosa Chemical Co., Ltd.
03 1Samung Industrial Co., Ltd.
01 3Sufentanil citrate
01 1Ireland
02 2U.S.A
Registrant Name : Samung Industrial Co., Ltd.
Registration Date : 2022-04-25
Registration Number : 20220421-210-J-1273(A)
Manufacturer Name : Macfarlan Smith Limited
Manufacturer Address : 10 Wheatfield Road, Edinburgh, EH11 2QA, United Kingdom
Registrant Name : Baeksu Pharmaceutical Co., Ltd.
Registration Date : 2022-04-21
Registration Number : 20220421-210-J-1273
Manufacturer Name : Macfarlan Smith Limited
Manufacturer Address : 10 Wheatfield Road, Edinburgh, EH11 2QA, United Kingdom
Registrant Name : Nosa Chemical Co., Ltd.
Registration Date : 2022-05-18
Registration Number : 20220518-210-J-1301
Manufacturer Name : SpecGx LLC
Manufacturer Address : 3600 North 2nd Street, St. Louis, MO 63147, USA
A Sufentanil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sufentanil, including repackagers and relabelers. The FDA regulates Sufentanil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sufentanil 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 Sufentanil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sufentanil supplier is an individual or a company that provides Sufentanil active pharmaceutical ingredient (API) or Sufentanil finished formulations upon request. The Sufentanil suppliers may include Sufentanil API manufacturers, exporters, distributors and traders.
click here to find a list of Sufentanil 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 Sufentanil Drug Master File in Korea (Sufentanil KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Sufentanil. The MFDS reviews the Sufentanil KDMF as part of the drug registration process and uses the information provided in the Sufentanil KDMF to evaluate the safety and efficacy of the drug.
After submitting a Sufentanil 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 Sufentanil API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Sufentanil suppliers with KDMF on PharmaCompass.
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