Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
01 1Pharmaceutical Works POLPHARMA S. A.
02 1Assia Chemical Industries Ltd.
03 1CHEMI S. p. A.
04 1Ipca Laboratories Limited
05 1Natco Pharma Limited.
06 1Nippon Kayaku Co., Ltd.
07 1Sanyo Fine Co., Ltd.
08 1ScinoPharm Taiwan, Ltd.
09 1Yung Shin Pharmaceutical Ind. Co. , Ltd.
01 5Zoledronic acid
02 1Zoledronic acid "CHEMI"
03 1Zoledronic acid hydrate
04 1Zoledronic acid hydrate "NK"
05 1Zoledronic acid hydrate "Teva"
01 1China
02 1Gabon
03 2India
04 1Israel
05 1Italy
06 1Japan
07 1Poland
08 1Taiwan
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
Registration Number : 225MF10034
Registrant's Address : 19 Pellinska Str. 83-200 Starogard Gdanski POLAND
Initial Date of Registration : 2013-02-20
Latest Date of Registration : 2017-06-15
Zoledronic Acid Hydrate "Teva"
Registration Number : 225MF10045
Registrant's Address : Neot-Hovav Eco-Industrial Park, Emek Sara P. O. Box 2049 Be'er Sheva 8412316, Israel
Initial Date of Registration : 2013-03-05
Latest Date of Registration : 2024-09-11
Registration Number : 225MF10022
Registrant's Address : Viale dei Laboratori 54, 20092 Cinisello Balsamo (Milano), Italy
Initial Date of Registration : 2013-02-06
Latest Date of Registration : 2013-02-06
Registration Number : 225MF10031
Registrant's Address : 48, Kandivli Industrial Estate, Kandivli (W), Mumbai 400 067, India
Initial Date of Registration : 2013-02-13
Latest Date of Registration : 2013-02-13
Registration Number : 225MF10053
Registrant's Address : Natco House, Road No. 2, Banjara Hills,Hyderabad 500034, Telangana, India
Initial Date of Registration : 2013-03-12
Latest Date of Registration : 2014-05-19
Registration Number : 225MF10012
Registrant's Address : 2-1-1 Marunouchi, Chiyoda-ku, Tokyo
Initial Date of Registration : 2013-01-30
Latest Date of Registration : 2013-11-14
Registration Number : 225MF10047
Registrant's Address : No. 1, Nan-Ke 8th Road, Shan-Hua, Tainan 74144 Taiwan
Initial Date of Registration : 2013-03-11
Latest Date of Registration : 2013-03-11
Registration Number : 227MF10043
Registrant's Address : Osaka Prefecture, Osaka City, Nishi Ward, Awaza 1-12-18
Initial Date of Registration : 2015-02-09
Latest Date of Registration : 2015-02-09
Registration Number : 225MF10058
Registrant's Address : No. 1191, Sec. 1, Chung Shan Rd. , Tachia, Taichung, Taiwan, R. O. C.
Initial Date of Registration : 2013-03-12
Latest Date of Registration : 2020-01-07
A Zoledronic Acid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zoledronic Acid, including repackagers and relabelers. The FDA regulates Zoledronic Acid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zoledronic Acid 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 Zoledronic Acid manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zoledronic Acid supplier is an individual or a company that provides Zoledronic Acid active pharmaceutical ingredient (API) or Zoledronic Acid finished formulations upon request. The Zoledronic Acid suppliers may include Zoledronic Acid API manufacturers, exporters, distributors and traders.
click here to find a list of Zoledronic Acid 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 Zoledronic Acid Drug Master File in Japan (Zoledronic Acid JDMF) empowers Zoledronic Acid 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 Zoledronic Acid JDMF during the approval evaluation for pharmaceutical products. At the time of Zoledronic Acid 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 Zoledronic Acid suppliers with JDMF on PharmaCompass.
We have 8 companies offering Zoledronic Acid
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