Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
01 1Granules India Limited
02 1Anqiu Lu'an Pharmaceutical Co. , Ltd.
03 1Atabay Kimya Sanayi ve Ticaret A. S.
04 1Farmson Basic Drugs Private Limited
05 1Hebei Jiheng (Group) Pharmaceutical Co. , Ltd. Shenzhou Plant
06 1Lianyungang Kangle Pharmaceutical Co. ,Ltd
07 2SHENZHOU JIHENG PHARMACEUTICAL CO. , LTD.
08 1SpecGx LLC
09 1SperaNexus Inc.
10 2Yamamoto Chemical Industry Co., Ltd.
11 4Yashiro Pharmaceutical Co., Ltd.
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
Registration Number : 228MF10061
Registrant's Address : 2nd Floor, 3rd Block, My Home Hub, Madhapur, Hyderabad, Telangana 500081 India
Initial Date of Registration : 2016-02-24
Latest Date of Registration : 2016-02-24
A Dolorol Forte manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dolorol Forte, including repackagers and relabelers. The FDA regulates Dolorol Forte manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dolorol Forte 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 Dolorol Forte manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dolorol Forte supplier is an individual or a company that provides Dolorol Forte active pharmaceutical ingredient (API) or Dolorol Forte finished formulations upon request. The Dolorol Forte suppliers may include Dolorol Forte API manufacturers, exporters, distributors and traders.
click here to find a list of Dolorol Forte 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 Dolorol Forte Drug Master File in Japan (Dolorol Forte JDMF) empowers Dolorol Forte 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 Dolorol Forte JDMF during the approval evaluation for pharmaceutical products. At the time of Dolorol Forte 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 Dolorol Forte suppliers with JDMF on PharmaCompass.
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