IKF/Pharmasynthese have been with fine chemicals market and APIs performance for more than 40 years.
01 1Pharmasynthesis SAS
02 1Pioneer Agro Industries (Pharmaceutical Division) Prop. Sanvin Laboratories Pvt. Ltd.
01 1Day stations dibucaine hydrochloride (production only)
02 1Divucine Hydrochloride
01 1France
02 1India
IKF/Pharmasynthese have been with fine chemicals market and APIs performance for more than 40 years.
Japanese Pharmacopoeia Dibucaine Hydrochloride (for manufacturing purposes only)
Registration Number : 218MF10076
Registrant's Address : 57, rue Gravetel St Pierre Les Elbeuf France
Initial Date of Registration : 2006-01-27
Latest Date of Registration : 2013-08-23
Registration Number : 303MF10086
Registrant's Address : 206, Eric House, 16th Road, Chembur, Mumbai-400071. INDIA.
Initial Date of Registration : 2021-06-03
Latest Date of Registration : 2021-06-03
A Dibucaine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dibucaine Hydrochloride, including repackagers and relabelers. The FDA regulates Dibucaine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dibucaine 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 Dibucaine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dibucaine Hydrochloride supplier is an individual or a company that provides Dibucaine Hydrochloride active pharmaceutical ingredient (API) or Dibucaine Hydrochloride finished formulations upon request. The Dibucaine Hydrochloride suppliers may include Dibucaine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Dibucaine Hydrochloride 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 Dibucaine Hydrochloride Drug Master File in Japan (Dibucaine Hydrochloride JDMF) empowers Dibucaine Hydrochloride 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 Dibucaine Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Dibucaine Hydrochloride JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Dibucaine Hydrochloride suppliers with JDMF on PharmaCompass.
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