01 1Cambrex Profarmaco Milano Srl@Sterilization process and freeze-drying contract manufacturing plant: Lampugnani Farmaceutici SPA
01 1Samoh Pharmaceutical Co., Ltd.
01 1Erythromycin lactobionate
01 1U.S.A
Registrant Name : Samoh Pharmaceutical Co., Ltd.
Registration Date : 2012-04-13
Registration Number : 20120413-107-F-61-01
Manufacturer Name : Cambrex Profarmaco Milano Sr...
Manufacturer Address : Via Curiel, 34, 20067 Paullo (MI) - ITALY@Vua Gransci 4 Nerviano (Milano), Italy
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PharmaCompass also assists you with knowing the Erythromycin Lactobionate API Price utilized in the formulation of products. Erythromycin Lactobionate API Price is not always fixed or binding as the Erythromycin Lactobionate Price is obtained through a variety of data sources. The Erythromycin Lactobionate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A C37H67NO13.C12H22O12 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of C37H67NO13.C12H22O12, including repackagers and relabelers. The FDA regulates C37H67NO13.C12H22O12 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. C37H67NO13.C12H22O12 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A C37H67NO13.C12H22O12 supplier is an individual or a company that provides C37H67NO13.C12H22O12 active pharmaceutical ingredient (API) or C37H67NO13.C12H22O12 finished formulations upon request. The C37H67NO13.C12H22O12 suppliers may include C37H67NO13.C12H22O12 API manufacturers, exporters, distributors and traders.
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In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a C37H67NO13.C12H22O12 Drug Master File in Korea (C37H67NO13.C12H22O12 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of C37H67NO13.C12H22O12. The MFDS reviews the C37H67NO13.C12H22O12 KDMF as part of the drug registration process and uses the information provided in the C37H67NO13.C12H22O12 KDMF to evaluate the safety and efficacy of the drug.
After submitting a C37H67NO13.C12H22O12 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 C37H67NO13.C12H22O12 API can apply through the Korea Drug Master File (KDMF).
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