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 1Hetero Labs Limited
04 2Industriale Chimica s.r.l.
05 1MSN Life Sciences Private Limited
06 1Optimus Drugs Private Limited
07 1Teva Czech Industries s.r.o
01 2OBETICHOLIC ACID
02 4Obeticholic Acid
03 1Obeticholic acid
04 1obeticholic acid
01 4India
02 1Israel
03 2Italy
04 1U.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 : 2026-12-31
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 : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 68554-0121
Start Marketing Date : 2016-05-27
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 63190-0840
Start Marketing Date : 2016-05-27
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 63190-0830
Start Marketing Date : 2016-05-27
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 69766-066
Start Marketing Date : 2019-02-28
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59285-028
Start Marketing Date : 2019-12-26
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 47848-056
Start Marketing Date : 2016-12-13
End Marketing Date : 2026-12-31
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, 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.
A IU6 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of IU6, including repackagers and relabelers. The FDA regulates IU6 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. IU6 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 IU6 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A IU6 supplier is an individual or a company that provides IU6 active pharmaceutical ingredient (API) or IU6 finished formulations upon request. The IU6 suppliers may include IU6 API manufacturers, exporters, distributors and traders.
click here to find a list of IU6 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 IU6 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for IU6 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 IU6 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 IU6 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a IU6 NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of IU6 suppliers with NDC on PharmaCompass.
We have 7 companies offering IU6
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