Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
01 1Biophore India Pharmaceuticals Private Limited
02 1Pharmacia & Upjohn Company LLC
03 1Curia Spain S.A.U.
04 1Hetero Labs Limited
05 2Industriale Chimica s.r.l.
06 1MSN Life Sciences Private Limited
07 1Optimus Drugs Private Limited
08 1Teva Czech Industries s.r.o
01 2OBETICHOLIC ACID
02 4Obeticholic Acid
03 2Obeticholic acid
04 1obeticholic acid
01 4India
02 1Israel
03 2Italy
04 2U.S.A
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 : 2025-12-31
Dosage Form (Strength) : POWDER (10kg/10kg)
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 : 69766-066
Start Marketing Date : 2019-02-28
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 : 2025-12-31
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
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PharmaCompass offers a list of Obeticholic 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 Obeticholic Acid manufacturer or Obeticholic Acid supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Obeticholic Acid manufacturer or Obeticholic Acid supplier.
PharmaCompass also assists you with knowing the Obeticholic Acid API Price utilized in the formulation of products. Obeticholic Acid API Price is not always fixed or binding as the Obeticholic Acid Price is obtained through a variety of data sources. The Obeticholic Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A OCALIVA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of OCALIVA, including repackagers and relabelers. The FDA regulates OCALIVA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. OCALIVA 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 OCALIVA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A OCALIVA supplier is an individual or a company that provides OCALIVA active pharmaceutical ingredient (API) or OCALIVA finished formulations upon request. The OCALIVA suppliers may include OCALIVA API manufacturers, exporters, distributors and traders.
click here to find a list of OCALIVA 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 OCALIVA as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for OCALIVA 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 OCALIVA 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 OCALIVA and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a OCALIVA NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of OCALIVA suppliers with NDC on PharmaCompass.
We have 8 companies offering OCALIVA
Get in contact with the supplier of your choice:
