Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
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Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
Registrant Name : Klasia Co., Ltd.
Registration Date : 2022-06-03
Registration Number : 20110429-40-C-279-18(2)
Manufacturer Name : Cohance Lifesciences Limited
Manufacturer Address : RS No.50/1, Mukteswarapuram Village, Jaggaiahpet Mandal, NTR District-521 457, Andhra...
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
Registrant Name : Hiple Co., Ltd.
Registration Date : 2016-05-02
Registration Number : 20090720-40-C-258-15(3)
Manufacturer Name : Granules India Limited
Manufacturer Address : Plot No 8, Jawaharlal Nehru Pharma City, Tadi Village, Parawada Mandal, Vitsakhapatna...
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
Registrant Name : Ace Biopharm Co., Ltd.
Registration Date : 2011-04-29
Registration Number : 20110429-40-C-279-18
Manufacturer Name : Cohance Lifesciences Limited
Manufacturer Address : RS No.50/1, Mukteswarapuram Village, Jaggaiahpet Mandal, NTR District-521 457, Andhra...
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
Registrant Name : Toru Corporation
Registration Date : 2020-01-30
Registration Number : 20110429-40-C-279-18(1)
Manufacturer Name : RA Chem Pharma Limited
Manufacturer Address : RS 50/1, Mukteswarapuram Village,Jaggaiahpeta Mandal, Krishna District-521 175. Andhr...
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
Registrant Name : Dongkwang Pharmaceutical Co., Ltd.
Registration Date : 2016-02-25
Registration Number : 20090720-40-C-258-15(2)
Manufacturer Name : Granules India Limited
Manufacturer Address : Plot No 8, Jawaharlal Nehru Pharma City, Tadi Village, Parawada Mandal, Vitsakhapatna...
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
Registrant Name : Kukjeon Pharmaceutical Co., Ltd.
Registration Date : 2009-07-20
Registration Number : 20090720-40-C-258-15
Manufacturer Name : Granules India Limited_x000D...
Manufacturer Address : Plot No 8, Jawaharlal Nehru Pharma City, Tadi Village, Parawada Mandal, Vitsakhapatna...
A Levocetirizine Dihydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Levocetirizine Dihydrochloride, including repackagers and relabelers. The FDA regulates Levocetirizine Dihydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Levocetirizine Dihydrochloride 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 Levocetirizine Dihydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Levocetirizine Dihydrochloride supplier is an individual or a company that provides Levocetirizine Dihydrochloride active pharmaceutical ingredient (API) or Levocetirizine Dihydrochloride finished formulations upon request. The Levocetirizine Dihydrochloride suppliers may include Levocetirizine Dihydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Levocetirizine Dihydrochloride 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 Levocetirizine Dihydrochloride Drug Master File in Korea (Levocetirizine Dihydrochloride KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Levocetirizine Dihydrochloride. The MFDS reviews the Levocetirizine Dihydrochloride KDMF as part of the drug registration process and uses the information provided in the Levocetirizine Dihydrochloride KDMF to evaluate the safety and efficacy of the drug.
After submitting a Levocetirizine Dihydrochloride 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 Levocetirizine Dihydrochloride API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Levocetirizine Dihydrochloride suppliers with KDMF on PharmaCompass.
We have 8 companies offering Levocetirizine Dihydrochloride
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