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01 2PharmaZell GmbH
02 2Dipharma Francis S.r.l.
03 1New Zealand Pharmaceuticals Limited
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01 1CHOLIC ACID
02 1CHOLIC ACID MICRONIZED
03 3Cholic acid
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01 2Germany
02 2Italy
03 1Blank
NDC Package Code : 12598-9622
Start Marketing Date : 2024-08-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12598-9642
Start Marketing Date : 2024-08-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46438-0669
Start Marketing Date : 2024-11-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46438-0670
Start Marketing Date : 2024-11-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 58979-001
Start Marketing Date : 2013-06-17
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Cholic Acid 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 Cholic Acid manufacturer or Cholic Acid supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cholic Acid manufacturer or Cholic Acid supplier.
PharmaCompass also assists you with knowing the Cholic Acid API Price utilized in the formulation of products. Cholic Acid API Price is not always fixed or binding as the Cholic Acid Price is obtained through a variety of data sources. The Cholic Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A C9377_SIGMA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of C9377_SIGMA, including repackagers and relabelers. The FDA regulates C9377_SIGMA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. C9377_SIGMA 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 C9377_SIGMA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A C9377_SIGMA supplier is an individual or a company that provides C9377_SIGMA active pharmaceutical ingredient (API) or C9377_SIGMA finished formulations upon request. The C9377_SIGMA suppliers may include C9377_SIGMA API manufacturers, exporters, distributors and traders.
click here to find a list of C9377_SIGMA 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 C9377_SIGMA as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for C9377_SIGMA 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 C9377_SIGMA 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 C9377_SIGMA and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a C9377_SIGMA NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of C9377_SIGMA suppliers with NDC on PharmaCompass.