Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.
01 1EGIS PHARMACEUTICALS PRIVATE LIMITED COMPANY
02 1Cheer Fine Pharmaceutical Co. , Ltd.
03 2Daiwa Pharmaceutical Industries Co., Ltd.
04 1Harman Finochem Ltd.
05 1Indoco Remedies Limited
06 2Sicor Societa (') Italiana Corticosteroidi S. r. l.
07 1Tianish Laboratories Private Limited
08 1Zhejiang Huayang Pharmaceutical Co., Ltd.
01 1ALLOPURINOL
02 4Allopurinol
03 1Allopurinol
04 1Allopurinol (C)
05 1Allopurinol (Teva / professional Syntex)
06 2Japanese Pharmacopoeia drugs allopurinol (production only)
01 2China
02 1Hungary
03 4India
04 2Italy
05 1U.S.A
Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.
Registration Number : 231MF10077
Registrant's Address : H-1106 BUDAPEST KERESZTURI UT 30-38 HUNGARY
Initial Date of Registration : 2019-03-29
Latest Date of Registration : 2019-03-29
Registration Number : 230MF10119
Registrant's Address : No. 2066 Tangkou Road, Economy and Technology Development Zone, Hefei, Anhui Province...
Initial Date of Registration : 2018-08-22
Latest Date of Registration : 2018-08-22
Japanese Pharmacopoeia Allopurinol (for manufacturing only)
Registration Number : 221MF10235
Registrant's Address : 2-3-5 Shimookui, Toyama City, Toyama Prefecture
Initial Date of Registration : 2009-10-29
Latest Date of Registration : 2018-11-05
Japanese Pharmacopoeia Allopurinol (for manufacturing only)
Registration Number : 217MF10496
Registrant's Address : 2-3-5 Shimookui, Toyama City, Toyama Prefecture
Initial Date of Registration : 2005-09-06
Latest Date of Registration : 2007-01-17
Registration Number : 231MF10078
Registrant's Address : 107-A, Vinay Bhavya Complex, 159-A, C. S. T Road, Kalina, Santa Cruz (East), Mumbai-4...
Initial Date of Registration : 2019-03-29
Latest Date of Registration : 2019-03-29
Registration Number : 225MF10144
Registrant's Address : 'Indoco House', 166 CST Road, Kalina, Santacruz (E) Mumbai-400 098 India
Initial Date of Registration : 2013-07-25
Latest Date of Registration : 2021-03-17
Registration Number : 301MF10064
Registrant's Address : Piazzale Luigi Cadorna, 4-20123 MILANO, Italy
Initial Date of Registration : 2019-09-17
Latest Date of Registration : 2020-09-17
Registration Number : 218MF10260
Registrant's Address : Piazzale Luigi Cadorna, 4-20123 MILANO, Italy
Initial Date of Registration : 2006-02-17
Latest Date of Registration : 2006-02-17
Registration Number : 217MF10578
Registrant's Address : Plot No. 564/A/22, Road No. 92, Jubilee Hills, Hyderabad-500096, Telangana, India
Initial Date of Registration : 2005-09-14
Latest Date of Registration : 2009-07-30
Registration Number : 221MF10137
Registrant's Address : No. 35, Donghai Fifth Avenue, Linhaiyuan District, Zhejiang Chemical Raw Materials Ba...
Initial Date of Registration : 2009-07-09
Latest Date of Registration : 2009-07-09
A Allopurinol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Allopurinol, including repackagers and relabelers. The FDA regulates Allopurinol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Allopurinol 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 Allopurinol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Allopurinol supplier is an individual or a company that provides Allopurinol active pharmaceutical ingredient (API) or Allopurinol finished formulations upon request. The Allopurinol suppliers may include Allopurinol API manufacturers, exporters, distributors and traders.
click here to find a list of Allopurinol 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 Allopurinol Drug Master File in Japan (Allopurinol JDMF) empowers Allopurinol 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 Allopurinol JDMF during the approval evaluation for pharmaceutical products. At the time of Allopurinol 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 Allopurinol suppliers with JDMF on PharmaCompass.
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