01 1DIFC CO. ,LTD
02 1ERCROS S. A.
03 1Ipca Laboratories Limited
04 2Ohara Pharmaceutical Co., Ltd.
05 1Phalanx Labs Private Limited
06 2Quimica Syntetica S. A.
07 2SMS Pharmaceuticals Limited
08 2Sanyo Chemical Research Institute Co., Ltd.
09 1UK Chemipharm Co. , Ltd.
10 2Yoshindo Co., Ltd.
01 1Day stations famotidine S (production only)
02 1FAMOTIDINE JP
03 8Famotidine
04 1Famotidine "PD" (production only)
05 1Famotidine (N)
06 1Famotidine JP (High Pure)
07 1Japanese Pharmacopoeia famotidine "D" (production only)
08 1Japanese Pharmacopoeia famotidine (production only)
01 1Egypt
02 2Gabon
03 4India
04 4Japan
05 1South Korea
06 3Spain
Registration Number : 223MF10054
Registrant's Address : A-501, SAMHO-MULSAN BLDG. 275-1 YANGJAE-DONG, SEOCHO-GU, SEOUL, KOREA
Initial Date of Registration : 2011-04-21
Latest Date of Registration : 2011-04-21
Registration Number : 226MF10186
Registrant's Address : Paseo del Deleite, s/n 28300-Aranjuez, Madrid Spain
Initial Date of Registration : 2014-09-30
Latest Date of Registration : 2016-03-11
Registration Number : 218MF10736
Registrant's Address : 48, Kandivli Industrial Estate, Kandivli (West), Mumbai 400 067, India
Initial Date of Registration : 2006-09-06
Latest Date of Registration : 2010-09-03
Famotidine "PD" (for manufacturing only)
Registration Number : 221MF10199
Registrant's Address : 121-15 Toriiino, Koka-cho, Koka City, Shiga Prefecture
Initial Date of Registration : 2009-09-14
Latest Date of Registration : 2009-09-14
Registration Number : 227MF10210
Registrant's Address : Gayatri Heights, Plot No. 9, Jaihind Enclave, Ayyappa Society, Madhapur, Hyderabad-50...
Initial Date of Registration : 2015-08-18
Latest Date of Registration : 2019-10-29
Registration Number : 227MF10091
Registrant's Address : Calle Dulcinea, s/n 28805 Alcala De Henares Madrid Spain
Initial Date of Registration : 2015-03-12
Latest Date of Registration : 2015-03-12
Registration Number : 226MF10116
Registrant's Address : Plot No. 72, H. No.:8-2-334/3&4 Road No. 5, Opp. SBI Executive Enclave, Banjara Hills...
Initial Date of Registration : 2014-06-18
Latest Date of Registration : 2015-01-05
Registration Number : 223MF10139
Registrant's Address : Plot No. 72, H. No.:8-2-334/3&4 Road No. 5, Opp. SBI Executive Enclave, Banjara Hills...
Initial Date of Registration : 2011-08-30
Latest Date of Registration : 2011-08-30
Registration Number : 221MF10253
Registrant's Address : 148-1 Tajii, Mihara-ku, Sakai City, Osaka Prefecture
Initial Date of Registration : 2009-11-24
Latest Date of Registration : 2009-11-24
Registration Number : 225MF10085
Registrant's Address : 3697-8 Hagishima, Funauchi-cho, Toyama City, Toyama Prefecture
Initial Date of Registration : 2013-04-23
Latest Date of Registration : 2014-05-29
A Famotidine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Famotidine, including repackagers and relabelers. The FDA regulates Famotidine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Famotidine 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 Famotidine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Famotidine supplier is an individual or a company that provides Famotidine active pharmaceutical ingredient (API) or Famotidine finished formulations upon request. The Famotidine suppliers may include Famotidine API manufacturers, exporters, distributors and traders.
click here to find a list of Famotidine 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 Famotidine Drug Master File in Japan (Famotidine JDMF) empowers Famotidine 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 Famotidine JDMF during the approval evaluation for pharmaceutical products. At the time of Famotidine 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 Famotidine suppliers with JDMF on PharmaCompass.
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