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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
01 3Cysteamine Bitartrate
02 1Cysteamine Bitartrate Hydrate
03 2Cysteamine bitartrate
01 1Canada
02 1Germany
03 1India
04 1Italy
05 1U.S.A
06 1Blank
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 : 2024-12-31
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 : 2024-12-31
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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A Cysteamine Bitartrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cysteamine Bitartrate, including repackagers and relabelers. The FDA regulates Cysteamine Bitartrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cysteamine Bitartrate 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 Bitartrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cysteamine Bitartrate supplier is an individual or a company that provides Cysteamine Bitartrate active pharmaceutical ingredient (API) or Cysteamine Bitartrate finished formulations upon request. The Cysteamine Bitartrate suppliers may include Cysteamine Bitartrate API manufacturers, exporters, distributors and traders.
click here to find a list of Cysteamine Bitartrate 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 Bitartrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Cysteamine Bitartrate 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 Bitartrate 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 Bitartrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Cysteamine Bitartrate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Cysteamine Bitartrate suppliers with NDC on PharmaCompass.
We have 5 companies offering Cysteamine Bitartrate
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