01 1Boehringer Ingelheim Pharma GmbH & Co. K.G.
01 1Boehringer Ingelheim Korea Ltd.
01 1Olodaterol hydrochloride
01 1Germany
Registrant Name : Boehringer Ingelheim Korea Ltd.
Registration Date : 2015-07-13
Registration Number : Number 2807-7-ND
Manufacturer Name : Boehringer Ingelheim Pharma ...
Manufacturer Address : Binger Straße 173, D-55216 Ingelheim, Germany
A Olodaterol Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Olodaterol Hydrochloride, including repackagers and relabelers. The FDA regulates Olodaterol Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Olodaterol Hydrochloride 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 Olodaterol Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Olodaterol Hydrochloride supplier is an individual or a company that provides Olodaterol Hydrochloride active pharmaceutical ingredient (API) or Olodaterol Hydrochloride finished formulations upon request. The Olodaterol Hydrochloride suppliers may include Olodaterol Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Olodaterol Hydrochloride 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 Olodaterol Hydrochloride Drug Master File in Korea (Olodaterol Hydrochloride KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Olodaterol Hydrochloride. The MFDS reviews the Olodaterol Hydrochloride KDMF as part of the drug registration process and uses the information provided in the Olodaterol Hydrochloride KDMF to evaluate the safety and efficacy of the drug.
After submitting a Olodaterol Hydrochloride 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 Olodaterol Hydrochloride API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Olodaterol Hydrochloride suppliers with KDMF on PharmaCompass.
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