Axplora- The partner of choice for complex APIs.
01 1PharmaZell GmbH
02 1Biophore India Pharmaceuticals Private Limited
03 1Dr. Reddy's Laboratories Limited
04 1Pharmacia & Upjohn Company LLC
05 1Curia Spain S.A.U.
06 1Hetero Labs Limited
07 2Industriale Chimica s.r.l.
08 1MSN Life Sciences Private Limited
09 1Optimus Drugs Private Limited
10 1Teva Czech Industries s.r.o
01 16-alpha-ethyl-chenodeoxycholic acid
02 2OBETICHOLIC ACID
03 5Obeticholic Acid
04 2Obeticholic acid
05 1obeticholic acid
01 1Germany
02 5India
03 1Israel
04 2Italy
05 2U.S.A
Axplora- The partner of choice for complex APIs.
NDC Package Code : 12598-5130
Start Marketing Date : 2010-10-25
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
NDC Package Code : 73435-004
Start Marketing Date : 2019-12-09
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (10kg/10kg)
Marketing Category : BULK INGREDIENT
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
NDC Package Code : 71796-004
Start Marketing Date : 2018-03-28
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Pfizer CentreOne is a global CDMO and a leading supplier of Specialty APIs.
NDC Package Code : 0009-0098
Start Marketing Date : 2021-05-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65089-0055
Start Marketing Date : 2016-05-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 68554-0121
Start Marketing Date : 2016-05-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 63190-0830
Start Marketing Date : 2016-05-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 63190-0840
Start Marketing Date : 2016-05-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59285-028
Start Marketing Date : 2019-12-26
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 47848-056
Start Marketing Date : 2016-12-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
A Obeticholic Acid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Obeticholic Acid, including repackagers and relabelers. The FDA regulates Obeticholic Acid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Obeticholic Acid 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 Obeticholic Acid manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Obeticholic Acid supplier is an individual or a company that provides Obeticholic Acid active pharmaceutical ingredient (API) or Obeticholic Acid finished formulations upon request. The Obeticholic Acid suppliers may include Obeticholic Acid API manufacturers, exporters, distributors and traders.
click here to find a list of Obeticholic Acid 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 Obeticholic Acid as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Obeticholic Acid 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 Obeticholic Acid 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 Obeticholic Acid and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Obeticholic Acid NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Obeticholic Acid suppliers with NDC on PharmaCompass.
We have 10 companies offering Obeticholic Acid
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