TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
01 1Teva API India Private Limited
02 1Almelo Pvt. Ltd.
03 1Cheer Fine Pharmaceutical Co. , Ltd.
04 1DONGBANG FUTURE TECH & LIFE CO. , LTD.
05 1HETERO DRUGS LIMITED.
06 1HIKAL LIMITED.
07 1Nantong Chanyoo Pharmatech Co. ,Ltd
08 1Saurav Chemicals Limited
09 1Sumitomo Chemical Co., Ltd.
01 8Pregabalin
02 1Pregabalin "Teva"
01 2China
02 4India
03 1Israel
04 1Japan
05 1South Korea
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Registration Number : 230MF10103
Registrant's Address : Plot No. 2G, 2H, 2I, Udyog Vihar, Greater Noida-201 308 (U.P.) India
Initial Date of Registration : 2018-08-08
Latest Date of Registration : 2022-06-15
Registration Number : 303MF10007
Registrant's Address : 8-2-120/45/A/2, Lane Opp. :Mayfair Apartments, Road No:2, Banjara Hills, Hyderabad, T...
Initial Date of Registration : 2021-01-14
Latest Date of Registration : 2021-01-14
Registration Number : 230MF10099
Registrant's Address : No. 2066 Tangkou Road, Economy and Technology Development Zone, Hefei, Anhui Province...
Initial Date of Registration : 2018-08-02
Latest Date of Registration : 2021-03-09
Registration Number : 230MF10092
Registrant's Address : 78, Jeyakgongdan 4-gil, Hyangnam-eup, Hwaseong-si, Gyeonggi-do, Korea
Initial Date of Registration : 2018-07-26
Latest Date of Registration : 2018-07-26
Registration Number : 230MF10102
Registrant's Address : 7-2-A2, Hetero Corporate, Industrial Estates, Sanath Nagar, Hyderabad-500 018, Telang...
Initial Date of Registration : 2018-08-08
Latest Date of Registration : 2018-08-08
Registration Number : 230MF10093
Registrant's Address : Great Eastern Chambers, CBD Belapur, Navi Mumbai-400 614, India
Initial Date of Registration : 2018-07-26
Latest Date of Registration : 2022-10-26
Registration Number : 230MF10118
Registrant's Address : #2 Tonghai Si Rd Yangkou Chemical Industrial Park Rudong Coastal Economic Development...
Initial Date of Registration : 2018-08-22
Latest Date of Registration : 2019-05-08
Registration Number : 230MF10100
Registrant's Address : Plot No. 370, Industrial Area, Phase-II, Panchkula, Haryana State, India
Initial Date of Registration : 2018-08-02
Latest Date of Registration : 2018-08-02
Registration Number : 230MF10072
Registrant's Address : 2-7-1 Nihonbashi, Chuo-ku, Tokyo
Initial Date of Registration : 2018-06-20
Latest Date of Registration : 2018-06-20
A Lyrica manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lyrica, including repackagers and relabelers. The FDA regulates Lyrica manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lyrica 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 Lyrica manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lyrica supplier is an individual or a company that provides Lyrica active pharmaceutical ingredient (API) or Lyrica finished formulations upon request. The Lyrica suppliers may include Lyrica API manufacturers, exporters, distributors and traders.
click here to find a list of Lyrica 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 Lyrica Drug Master File in Japan (Lyrica JDMF) empowers Lyrica 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 Lyrica JDMF during the approval evaluation for pharmaceutical products. At the time of Lyrica 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 Lyrica suppliers with JDMF on PharmaCompass.
We have 9 companies offering Lyrica
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
