IKF/Pharmasynthese have been with fine chemicals market and APIs performance for more than 40 years.
Reset all filters
01 1PHARMASYNTHESE
02 1Zhejiang Hisoar Pharmaceutical Co., Ltd
Reset all filters
01 1Ace Biopharm Co., Ltd.
02 1Toru Corporation
Reset all filters
01 2Amorolfine hydrochloride
Reset all filters
01 1China
02 1France
IKF/Pharmasynthese have been with fine chemicals market and APIs performance for more than 40 years.
Registrant Name : Toru Corporation
Registration Date : 2021-06-02
Registration Number : 20210602-211-J-1005
Manufacturer Name : PHARMASYNTHESE
Manufacturer Address : 57, rue Gravetel-BP3 76320 SAINT-PIERRE-LES-ELBEUF, France
Registrant Name : Ace Biopharm Co., Ltd.
Registration Date : 2019-12-04
Registration Number : 20191204-211-J-495
Manufacturer Name : Zhejiang Hisoar Pharmaceutic...
Manufacturer Address : No. 100 Waisha Branch Road. Jiaojiang, Taizhou, China
A Locetar manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Locetar, including repackagers and relabelers. The FDA regulates Locetar manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Locetar 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 Locetar manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Locetar supplier is an individual or a company that provides Locetar active pharmaceutical ingredient (API) or Locetar finished formulations upon request. The Locetar suppliers may include Locetar API manufacturers, exporters, distributors and traders.
click here to find a list of Locetar 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 Locetar Drug Master File in Korea (Locetar KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Locetar. The MFDS reviews the Locetar KDMF as part of the drug registration process and uses the information provided in the Locetar KDMF to evaluate the safety and efficacy of the drug.
After submitting a Locetar 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 Locetar API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Locetar suppliers with KDMF on PharmaCompass.
We have 2 companies offering Locetar
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?