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 Sodium liothyronine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sodium liothyronine, including repackagers and relabelers. The FDA regulates Sodium liothyronine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sodium liothyronine 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 Sodium liothyronine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Sodium liothyronine supplier is an individual or a company that provides Sodium liothyronine active pharmaceutical ingredient (API) or Sodium liothyronine finished formulations upon request. The Sodium liothyronine suppliers may include Sodium liothyronine API manufacturers, exporters, distributors and traders.
click here to find a list of Sodium liothyronine 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 Sodium liothyronine Drug Master File in Korea (Sodium liothyronine KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Sodium liothyronine. The MFDS reviews the Sodium liothyronine KDMF as part of the drug registration process and uses the information provided in the Sodium liothyronine KDMF to evaluate the safety and efficacy of the drug.
After submitting a Sodium liothyronine 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 Sodium liothyronine API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Sodium liothyronine suppliers with KDMF on PharmaCompass.
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