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01 1Farmabios SPA@MICROCHEM SRL
01 1Samil Pharmaceutical Co., Ltd.
01 1Micronized fludrocortisone acetate
01 1Germany
Micronized fludrocortisone acetate
Registrant Name : Samil Pharmaceutical Co., Ltd.
Registration Date : 2021-12-02
Registration Number : 20211202-209-J-1149
Manufacturer Name : Farmabios SPA@MICROCHEM SRL
Manufacturer Address : Via Pavia 1 - 27027 Gropello Cairoli (PV), Italy@Via Turati, 2 - 29017 Fiorenzuola d'...
A Fludrocortisone Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fludrocortisone Acetate, including repackagers and relabelers. The FDA regulates Fludrocortisone Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fludrocortisone Acetate 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 Fludrocortisone Acetate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fludrocortisone Acetate supplier is an individual or a company that provides Fludrocortisone Acetate active pharmaceutical ingredient (API) or Fludrocortisone Acetate finished formulations upon request. The Fludrocortisone Acetate suppliers may include Fludrocortisone Acetate API manufacturers, exporters, distributors and traders.
click here to find a list of Fludrocortisone Acetate 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 Fludrocortisone Acetate Drug Master File in Korea (Fludrocortisone Acetate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Fludrocortisone Acetate. The MFDS reviews the Fludrocortisone Acetate KDMF as part of the drug registration process and uses the information provided in the Fludrocortisone Acetate KDMF to evaluate the safety and efficacy of the drug.
After submitting a Fludrocortisone Acetate 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 Fludrocortisone Acetate API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Fludrocortisone Acetate suppliers with KDMF on PharmaCompass.
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