01 1Indoco Remedies Limited
01 1Dicyclomine hydrochloride
01 1India
Registration Number : 226MF10115
Registrant's Address : 'Indoco House', 166 CST Road, Kalina, Santacruz (E) Mumbai-400 098 India.
Initial Date of Registration : 2014-06-18
Latest Date of Registration : 2022-06-22
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PharmaCompass offers a list of Dicyclomine Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Dicyclomine Hydrochloride manufacturer or Dicyclomine Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Dicyclomine Hydrochloride API Price utilized in the formulation of products. Dicyclomine Hydrochloride API Price is not always fixed or binding as the Dicyclomine Hydrochloride Price is obtained through a variety of data sources. The Dicyclomine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Dicycloverine hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dicycloverine hydrochloride, including repackagers and relabelers. The FDA regulates Dicycloverine hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dicycloverine 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.
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A Dicycloverine hydrochloride supplier is an individual or a company that provides Dicycloverine hydrochloride active pharmaceutical ingredient (API) or Dicycloverine hydrochloride finished formulations upon request. The Dicycloverine hydrochloride suppliers may include Dicycloverine hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Dicycloverine 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 Dicycloverine hydrochloride Drug Master File in Japan (Dicycloverine hydrochloride JDMF) empowers Dicycloverine 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 Dicycloverine hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Dicycloverine hydrochloride 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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