01 1PIONEER AGRO INDUSTRIES SANVIN LABORATORIES PRIVATE LIMITED
01 1Japanese Pharmacopoeia cyclopentolate hydrochloride
01 1India
Japanese Pharmacopoeia Cyclopentolate Hydrochloride
Registration Number : 222MF10222
Registrant's Address : 206, Eric House, 16th Road, Chembur, Mumbai-400071. INDIA.
Initial Date of Registration : 2010-08-26
Latest Date of Registration : 2020-01-24
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PharmaCompass offers a list of Cyclopentolate 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 Cyclopentolate Hydrochloride manufacturer or Cyclopentolate Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cyclopentolate Hydrochloride manufacturer or Cyclopentolate Hydrochloride supplier.
PharmaCompass also assists you with knowing the Cyclopentolate Hydrochloride API Price utilized in the formulation of products. Cyclopentolate Hydrochloride API Price is not always fixed or binding as the Cyclopentolate Hydrochloride Price is obtained through a variety of data sources. The Cyclopentolate Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Zyklolat manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zyklolat, including repackagers and relabelers. The FDA regulates Zyklolat manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zyklolat 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 Zyklolat supplier is an individual or a company that provides Zyklolat active pharmaceutical ingredient (API) or Zyklolat finished formulations upon request. The Zyklolat suppliers may include Zyklolat API manufacturers, exporters, distributors and traders.
click here to find a list of Zyklolat 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 Zyklolat Drug Master File in Japan (Zyklolat JDMF) empowers Zyklolat 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 Zyklolat JDMF during the approval evaluation for pharmaceutical products. At the time of Zyklolat 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 Zyklolat suppliers with JDMF on PharmaCompass.
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