Bal Pharma, leading manufacturer of niche & specialty API, Intermediates and Finished Formulations.
01 1Bal Pharma Limited
02 1AARTI INDUSTRIES LIMITED.
03 1Glenmark Life Sciences Limited
04 1MEDICHEM S. A.
05 1Olon S. p. A.
06 1Tateyama Chemical Co., Ltd.
01 5Adapalene
02 1Adapalene "Tateyama"
01 1Gabon
02 3India
03 1Italy
04 1Japan
Registration Number : 228MF10176
Registrant's Address : 5th Floor, Lakshminarayan Complex, 10/1, Palace Road, Bangalore-560052, India
Initial Date of Registration : 2016-08-29
Latest Date of Registration : 2021-03-09
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Registration Number : 228MF10126
Registrant's Address : 71, UDYOG KSHETRA, ULND-GOREGAON LINK ROAD, MULUND (W), MUMBAI 400080, INDIA
Initial Date of Registration : 2016-07-13
Latest Date of Registration : 2016-07-13
Registration Number : 226MF10072
Registrant's Address : 4th Floor, OIA House, 470, Cardinal Gracious Road, Andheri East Mumbai 400099, Mahara...
Initial Date of Registration : 2014-03-11
Latest Date of Registration : 2017-05-16
Registration Number : 228MF10145
Registrant's Address : Strada Rivoltana km. 6/7 20053 Rodano (MI), Italy
Initial Date of Registration : 2016-08-03
Latest Date of Registration : 2019-12-20
Registration Number : 228MF10167
Registrant's Address : 1133 Oe, Imizu City, Toyama Prefecture
Initial Date of Registration : 2016-08-19
Latest Date of Registration : 2021-01-20
Registration Number : 228MF10149
Registrant's Address : 6-8, Fructo(´)s Gelabert 08970 Sant Joan Despi(´)(Barcelona)Spain
Initial Date of Registration : 2016-08-03
Latest Date of Registration : 2016-08-03
A Adapalene manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Adapalene, including repackagers and relabelers. The FDA regulates Adapalene manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Adapalene 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 Adapalene manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Adapalene supplier is an individual or a company that provides Adapalene active pharmaceutical ingredient (API) or Adapalene finished formulations upon request. The Adapalene suppliers may include Adapalene API manufacturers, exporters, distributors and traders.
click here to find a list of Adapalene 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 Adapalene Drug Master File in Japan (Adapalene JDMF) empowers Adapalene 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 Adapalene JDMF during the approval evaluation for pharmaceutical products. At the time of Adapalene 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 Adapalene suppliers with JDMF on PharmaCompass.
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