IKF/Pharmasynthese have been with fine chemicals market and APIs performance for more than 40 years.
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01 1PHARMASYNTHESE
02 1Zhejiang Hisoar Pharmaceutical Co., Ltd
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01 1Ace Biopharm Co., Ltd.
02 1Toru Corporation
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01 2Amorolfine hydrochloride
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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 Amorolfine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Amorolfine, including repackagers and relabelers. The FDA regulates Amorolfine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Amorolfine 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 Amorolfine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Amorolfine supplier is an individual or a company that provides Amorolfine active pharmaceutical ingredient (API) or Amorolfine finished formulations upon request. The Amorolfine suppliers may include Amorolfine API manufacturers, exporters, distributors and traders.
click here to find a list of Amorolfine 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 Amorolfine Drug Master File in Korea (Amorolfine KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Amorolfine. The MFDS reviews the Amorolfine KDMF as part of the drug registration process and uses the information provided in the Amorolfine KDMF to evaluate the safety and efficacy of the drug.
After submitting a Amorolfine 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 Amorolfine API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Amorolfine suppliers with KDMF on PharmaCompass.
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