01 1AMERICAN PACIFIC CORPORATION
02 1Darmerica
03 1Kekule Life Sciences Limited
04 1Sionc Pharmaceutical Private Limited
01 2CHLORAMBUCIL
02 2Chlorambucil
01 1India
02 2U.S.A
03 1Blank
NDC Package Code : 50683-0384
Start Marketing Date : 2001-05-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 71052-212
Start Marketing Date : 2017-04-01
End Marketing Date : 2027-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 76055-0025
Start Marketing Date : 2019-12-28
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 87358-123
Start Marketing Date : 2026-01-21
End Marketing Date : 2027-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Chlorambucil API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Chlorambucil manufacturer or Chlorambucil supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Chlorambucil manufacturer or Chlorambucil supplier.
A CCG-39872 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CCG-39872, including repackagers and relabelers. The FDA regulates CCG-39872 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CCG-39872 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 CCG-39872 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A CCG-39872 supplier is an individual or a company that provides CCG-39872 active pharmaceutical ingredient (API) or CCG-39872 finished formulations upon request. The CCG-39872 suppliers may include CCG-39872 API manufacturers, exporters, distributors and traders.
click here to find a list of CCG-39872 suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 CCG-39872 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for CCG-39872 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 CCG-39872 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 CCG-39872 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a CCG-39872 NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of CCG-39872 suppliers with NDC on PharmaCompass.
We have 3 companies offering CCG-39872
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