01 1Shandong Anhong Pharmaceutical Co. , Ltd.
01 1Ropivacaine Hydrochloride Hydrate
01 1China
Ropivacaine hydrochloride hydrate
Registration Number : 305MF10079
Registrant's Address : No. 29 Huayuan Street Linyi County, Dezhou, Shandong, China
Initial Date of Registration : 2023-07-12
Latest Date of Registration : 2023-07-12
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PharmaCompass also assists you with knowing the Ropivacaine Hydrochloride API Price utilized in the formulation of products. Ropivacaine Hydrochloride API Price is not always fixed or binding as the Ropivacaine Hydrochloride Price is obtained through a variety of data sources. The Ropivacaine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A AstraZeneca brand of ropivacaine monohydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AstraZeneca brand of ropivacaine monohydrochloride, including repackagers and relabelers. The FDA regulates AstraZeneca brand of ropivacaine monohydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AstraZeneca brand of ropivacaine monohydrochloride 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 AstraZeneca brand of ropivacaine monohydrochloride supplier is an individual or a company that provides AstraZeneca brand of ropivacaine monohydrochloride active pharmaceutical ingredient (API) or AstraZeneca brand of ropivacaine monohydrochloride finished formulations upon request. The AstraZeneca brand of ropivacaine monohydrochloride suppliers may include AstraZeneca brand of ropivacaine monohydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of AstraZeneca brand of ropivacaine monohydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The AstraZeneca brand of ropivacaine monohydrochloride Drug Master File in Japan (AstraZeneca brand of ropivacaine monohydrochloride JDMF) empowers AstraZeneca brand of ropivacaine monohydrochloride API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the AstraZeneca brand of ropivacaine monohydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of AstraZeneca brand of ropivacaine monohydrochloride JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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