Inke S.A: APIs manufacturing plant.
01 1Inke S.A.
02 1CADILA PHARMACEUTICALS LIMITED.
03 1Daito Co., Ltd.
04 1Morepen Laboratories Limited
05 1Tianish Laboratories Private Limited
06 1Vasudha Pharma Chem Limited
01 5Loratadine
02 1Loratadine (production only)
01 3India
02 1Japan
03 1Spain
04 1U.S.A
Inke S.A: APIs manufacturing plant.
Registration Number : 222MF10170
Registrant's Address : Area Industrial del Llobregat, C/Argent 1,08755 Castellbisbal Barcelona SPAIN
Initial Date of Registration : 2010-06-08
Latest Date of Registration : 2010-06-08
Loratadine (for manufacturing purposes only)
Registration Number : 222MF10187
Registrant's Address : Sarkhej-Dholka Road, Bhat, Ahmedabad-382 210, Gujarat, INDIA
Initial Date of Registration : 2010-07-02
Latest Date of Registration : 2017-06-21
Registration Number : 222MF10175
Registrant's Address : 326 Yokamachi, Toyama City, Toyama Prefecture
Initial Date of Registration : 2010-06-18
Latest Date of Registration : 2021-08-16
Registration Number : 227MF10263
Registrant's Address : 2nd Floor, Tower C, DLF Cyber Park, Udyog Vihar, Sector-20, Gurugram-Haryana, 1...
Initial Date of Registration : 2015-11-11
Latest Date of Registration : 2021-10-13
Registration Number : 306MF10126
Registrant's Address : 78/A, Bengalrao Nagar, Hyderabad 500 038, Telangana State, India.
Initial Date of Registration : 2024-09-18
Latest Date of Registration : 2024-09-18
Registration Number : 220MF10191
Registrant's Address : Plot No. 564/A/22, Road No. 92, Jubilee Hills, Hyderabad-500096, Telangana, India
Initial Date of Registration : 2008-08-18
Latest Date of Registration : 2018-06-14
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PharmaCompass offers a list of Loratadine 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 Loratadine manufacturer or Loratadine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Loratadine manufacturer or Loratadine supplier.
PharmaCompass also assists you with knowing the Loratadine API Price utilized in the formulation of products. Loratadine API Price is not always fixed or binding as the Loratadine Price is obtained through a variety of data sources. The Loratadine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A L 9664 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of L 9664, including repackagers and relabelers. The FDA regulates L 9664 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. L 9664 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 L 9664 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A L 9664 supplier is an individual or a company that provides L 9664 active pharmaceutical ingredient (API) or L 9664 finished formulations upon request. The L 9664 suppliers may include L 9664 API manufacturers, exporters, distributors and traders.
click here to find a list of L 9664 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 L 9664 Drug Master File in Japan (L 9664 JDMF) empowers L 9664 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 L 9664 JDMF during the approval evaluation for pharmaceutical products. At the time of L 9664 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 L 9664 suppliers with JDMF on PharmaCompass.
We have 6 companies offering L 9664
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