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01 1Teva API India Ltd
01 1Samoh Pharmaceutical Co., Ltd.
01 1Sitagliptin malate
01 1Israel
Registrant Name : Samoh Pharmaceutical Co., Ltd.
Registration Date : 2016-01-05
Registration Number : 2991-24-ND
Manufacturer Name : Teva API India Ltd
Manufacturer Address : Plot No. Q.1 to 4, Industrial Area, Ghirongi, Malanpur, Distt. Behind (MP) India_x000...
A Sitagliptin Malate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sitagliptin Malate, including repackagers and relabelers. The FDA regulates Sitagliptin Malate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sitagliptin Malate 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 Sitagliptin Malate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sitagliptin Malate supplier is an individual or a company that provides Sitagliptin Malate active pharmaceutical ingredient (API) or Sitagliptin Malate finished formulations upon request. The Sitagliptin Malate suppliers may include Sitagliptin Malate API manufacturers, exporters, distributors and traders.
click here to find a list of Sitagliptin Malate 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 Sitagliptin Malate Drug Master File in Korea (Sitagliptin Malate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Sitagliptin Malate. The MFDS reviews the Sitagliptin Malate KDMF as part of the drug registration process and uses the information provided in the Sitagliptin Malate KDMF to evaluate the safety and efficacy of the drug.
After submitting a Sitagliptin Malate 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 Sitagliptin Malate API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Sitagliptin Malate suppliers with KDMF on PharmaCompass.
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