 Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
 
										

 
				
									 
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01 1FARMAK, a. s.
02 1SANOFI WINTHROP INDUSTRIE
03 1Teva API India Private Limited
04 2Active Pharma Co., Ltd.
05 1Alives Life Sciences Limited
06 1Assia Chemical Industries Ltd.
07 1CENTAUR PHARMACEUTICALS PRIVATE LTD.
08 1LUPIN LIMITED.
09 2Permakem Asia Co., Ltd.
10 1Tianish Laboratories Private Limited
									 
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01 1Japanese Pharmacopoeia Zolpidem Tartrate
02 2Zolpidem Tartrate
03 6Zolpidem tartrate
04 1Zolpidem tartrate
05 1Zolpidem tartrate "Teva"
06 1Zolpidem tartrate "unground product"
									 
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01 1Czech Republic
02 1France
03 3India
04 2Israel
05 4Japan
06 1U.S.A
 Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
Registration Number : 218MF10589
Registrant's Address : Na vlcinci 16/3 Klasterni Hradisko 779 00 Olomouc Czech Republic
Initial Date of Registration : 2006-06-22
Latest Date of Registration : 2025-07-03
Registration Number : 219MF10328
Registrant's Address : 82 Avenue Raspail 94250 Gentilly (FRANCE)
Initial Date of Registration : 2007-11-05
Latest Date of Registration : 2013-12-03
 TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Registration Number : 306MF10046
Registrant's Address : Plot No. 2G, 2H, 2I, Udyog Vihar, Greater Noida-201 308 (U.P.) India
Initial Date of Registration : 2024-03-21
Latest Date of Registration : 2024-03-21
 
											 
												Registration Number : 227MF10247
Registrant's Address : 2-36-1 Kanda Jinbocho, Chiyoda-ku, Tokyo
Initial Date of Registration : 2015-10-08
Latest Date of Registration : 2015-10-08

 
											 
												Registration Number : 227MF10236
Registrant's Address : 4th Floor, OIA House, 470, Cardinal Gracious Road, Andheri East Mumbai 400099, Mahara...
Initial Date of Registration : 2015-09-24
Latest Date of Registration : 2019-04-11

 
											 
												Registration Number : 301MF10096
Registrant's Address : “CENTAUR HOUSE”, NEAR GRAND HYATT, SHANTI NAGAR, VAKOLA, SANTACRUZ (EAST), MUMBAI...
Initial Date of Registration : 2019-11-19
Latest Date of Registration : 2019-11-19

 
											 
												Registration Number : 222MF10220
Registrant's Address : 159, CST Road, Kalina, Santacruz (East) Mumbai-400 098, INDIA
Initial Date of Registration : 2010-08-16
Latest Date of Registration : 2010-08-16

 
											 
												Registration Number : 223MF10007
Registrant's Address : 1-10-11 Horidomecho, Chuo-ku, Tokyo
Initial Date of Registration : 2011-01-14
Latest Date of Registration : 2011-01-14

 
											 
												Registration Number : 222MF10264
Registrant's Address : 1-10-11 Horidomecho, Chuo-ku, Tokyo
Initial Date of Registration : 2010-11-29
Latest Date of Registration : 2010-11-29

 
											 
												Japanese Pharmacopoeia Zolpidem Tartrate
Registration Number : 230MF10139
Registrant's Address : Plot No. 564/A/22, Road No. 92, Jubilee Hills, Hyderabad-500096, Telangana, India
Initial Date of Registration : 2018-10-12
Latest Date of Registration : 2018-10-12

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PharmaCompass offers a list of Zolpidem Tartrate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Zolpidem Tartrate manufacturer or Zolpidem Tartrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Zolpidem Tartrate manufacturer or Zolpidem Tartrate supplier.
PharmaCompass also assists you with knowing the Zolpidem Tartrate API Price utilized in the formulation of products. Zolpidem Tartrate API Price is not always fixed or binding as the Zolpidem Tartrate Price is obtained through a variety of data sources. The Zolpidem Tartrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Zolpimist manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zolpimist, including repackagers and relabelers. The FDA regulates Zolpimist manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zolpimist 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 Zolpimist manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zolpimist supplier is an individual or a company that provides Zolpimist active pharmaceutical ingredient (API) or Zolpimist finished formulations upon request. The Zolpimist suppliers may include Zolpimist API manufacturers, exporters, distributors and traders.
click here to find a list of Zolpimist 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 Zolpimist Drug Master File in Japan (Zolpimist JDMF) empowers Zolpimist 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 Zolpimist JDMF during the approval evaluation for pharmaceutical products. At the time of Zolpimist 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 Zolpimist suppliers with JDMF on PharmaCompass.
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