01 EPAX NORWAY AS (1)
02 SAFC (1)
03 SIGMA TAU (1)
01 BUTYRIC ACID (1)
02 EPAX 4608 EE US PH (EPA-ENRICHED FATTY ACID ETHYL ESTER) (1)
03 L-AMINO-n-BUTYRIC ACID (1)
01 Norway (1)
02 U.S.A (2)
01 Active (1)
02 Inactive (2)
01 Blank (3)
28
PharmaCompass offers a list of Sodium Butyrate 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 Sodium Butyrate manufacturer or Sodium Butyrate supplier for your needs.
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PharmaCompass also assists you with knowing the Sodium Butyrate API Price utilized in the formulation of products. Sodium Butyrate API Price is not always fixed or binding as the Sodium Butyrate Price is obtained through a variety of data sources. The Sodium Butyrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tox21_202382 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_202382, including repackagers and relabelers. The FDA regulates Tox21_202382 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_202382 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 Tox21_202382 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tox21_202382 supplier is an individual or a company that provides Tox21_202382 active pharmaceutical ingredient (API) or Tox21_202382 finished formulations upon request. The Tox21_202382 suppliers may include Tox21_202382 API manufacturers, exporters, distributors and traders.
click here to find a list of Tox21_202382 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tox21_202382 DMF (Drug Master File) is a document detailing the whole manufacturing process of Tox21_202382 active pharmaceutical ingredient (API) in detail. Different forms of Tox21_202382 DMFs exist exist since differing nations have different regulations, such as Tox21_202382 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Tox21_202382 DMF submitted to regulatory agencies in the US is known as a USDMF. Tox21_202382 USDMF includes data on Tox21_202382's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Tox21_202382 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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