01 1Azico Biophore India Private Limited
01 1Aging Life Science Co., Ltd.
01 1Liothironin sodium
01 1India
Registrant Name : Aging Life Science Co., Ltd.
Registration Date : 2020-11-25
Registration Number : 20201125-211-J-790
Manufacturer Name : Azico Biophore India Private...
Manufacturer Address : Plot Number 40/A, Sy. No. 13,15,16,51,52 & 182, JN.Pharma city, Thanam(V), Anakapalli...
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PharmaCompass offers a list of Liothyronine Sodium API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Liothyronine Sodium manufacturer or Liothyronine Sodium supplier for your needs.
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A Liothyronin sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Liothyronin sodium, including repackagers and relabelers. The FDA regulates Liothyronin sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Liothyronin sodium 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 Liothyronin sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Liothyronin sodium supplier is an individual or a company that provides Liothyronin sodium active pharmaceutical ingredient (API) or Liothyronin sodium finished formulations upon request. The Liothyronin sodium suppliers may include Liothyronin sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Liothyronin sodium suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Liothyronin sodium Drug Master File in Korea (Liothyronin sodium KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Liothyronin sodium. The MFDS reviews the Liothyronin sodium KDMF as part of the drug registration process and uses the information provided in the Liothyronin sodium KDMF to evaluate the safety and efficacy of the drug.
After submitting a Liothyronin sodium 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 Liothyronin sodium API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Liothyronin sodium suppliers with KDMF on PharmaCompass.
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