Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
01 1Farmak, a,s
02 1AARTI DRUGS LTD
03 1Assia Chemical Industries Ltd - Teva Tech Site
04 1Aurobindo Pharma Limited
05 1Cambrex Profarmaco Milano Srl
06 2Glenmark Life Sciences Limited
07 1MYLAN LABORATORIES LIMITED
08 1Tianish Laboratories Private Limited
09 1Unichem Laboratories Limited, India
10 1Uquifa Mexico, S.A. DE C.V.
01 2ZOLPIDEM TARTRATE
02 9Zolpidem Tartrate
01 1Czech Republic
02 6India
03 1Israel
04 1Spain
05 2U.S.A
Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
NDC Package Code : 63278-0490
Start Marketing Date : 2006-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62704-0113
Start Marketing Date : 2006-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 63415-0081
Start Marketing Date : 2022-03-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65862-345
Start Marketing Date : 2023-12-11
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12828-0086
Start Marketing Date : 2012-06-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 66039-938
Start Marketing Date : 2005-03-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 66039-810
Start Marketing Date : 2005-03-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 53747-017
Start Marketing Date : 2007-12-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 52286-0004
Start Marketing Date : 2009-11-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65015-767
Start Marketing Date : 2015-01-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Zolpidem manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zolpidem, including repackagers and relabelers. The FDA regulates Zolpidem manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zolpidem 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 Zolpidem manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zolpidem supplier is an individual or a company that provides Zolpidem active pharmaceutical ingredient (API) or Zolpidem finished formulations upon request. The Zolpidem suppliers may include Zolpidem API manufacturers, exporters, distributors and traders.
click here to find a list of Zolpidem suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Zolpidem as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Zolpidem API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Zolpidem as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Zolpidem and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Zolpidem NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Zolpidem suppliers with NDC on PharmaCompass.
We have 10 companies offering Zolpidem
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