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01 1Farmabios S.p.A.
02 1AX Pharmaceutical Corp
03 1Anonima Materie Sintetiche and Affini (AMSA) Spa
04 1Cambrex Profarmaco Milano Srl
05 1HOSTER LABS PRIVATE LIMITED
06 1Maithri Laboratories Private Limited
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01 3Cysteamine Bitartrate
02 1Cysteamine Bitartrate Hydrate
03 2Cysteamine bitartrate
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01 1Canada
02 1Germany
03 1India
04 1Italy
05 1U.S.A
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NDC Package Code : 46439-8762
Start Marketing Date : 2018-05-22
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17373-1199
Start Marketing Date : 2022-10-18
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 73377-300
Start Marketing Date : 2024-11-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 12828-0068
Start Marketing Date : 1993-02-22
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 71666-010
Start Marketing Date : 2020-04-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 82708-0007
Start Marketing Date : 1994-08-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Cysteamine Bitartrate 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 Cysteamine Bitartrate manufacturer or Cysteamine Bitartrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cysteamine Bitartrate manufacturer or Cysteamine Bitartrate supplier.
PharmaCompass also assists you with knowing the Cysteamine Bitartrate API Price utilized in the formulation of products. Cysteamine Bitartrate API Price is not always fixed or binding as the Cysteamine Bitartrate Price is obtained through a variety of data sources. The Cysteamine Bitartrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cysteamine Tartrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cysteamine Tartrate, including repackagers and relabelers. The FDA regulates Cysteamine Tartrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cysteamine Tartrate 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 Cysteamine Tartrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cysteamine Tartrate supplier is an individual or a company that provides Cysteamine Tartrate active pharmaceutical ingredient (API) or Cysteamine Tartrate finished formulations upon request. The Cysteamine Tartrate suppliers may include Cysteamine Tartrate API manufacturers, exporters, distributors and traders.
click here to find a list of Cysteamine Tartrate 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 Cysteamine Tartrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Cysteamine Tartrate 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 Cysteamine Tartrate 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 Cysteamine Tartrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Cysteamine Tartrate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Cysteamine Tartrate suppliers with NDC on PharmaCompass.
We have 5 companies offering Cysteamine Tartrate
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