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 Acetaminophen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Acetaminophen, including repackagers and relabelers. The FDA regulates Acetaminophen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Acetaminophen 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 Acetaminophen manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Acetaminophen supplier is an individual or a company that provides Acetaminophen active pharmaceutical ingredient (API) or Acetaminophen finished formulations upon request. The Acetaminophen suppliers may include Acetaminophen API manufacturers, exporters, distributors and traders.
click here to find a list of Acetaminophen 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 Acetaminophen Drug Master File in Japan (Acetaminophen JDMF) empowers Acetaminophen 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 Acetaminophen JDMF during the approval evaluation for pharmaceutical products. At the time of Acetaminophen 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 Acetaminophen suppliers with JDMF on PharmaCompass.
We have 10 companies offering Acetaminophen
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
