Pfanstiehl, a global leader in the manufacture of cGMP high purity, low endotoxin, low metals (HPLE-LM)TM injectable grade excipients.
01 1Pfanstiehl
01 1SUCCINIC ACID, HIGH PURITY, LOW ENDOTOXIN, LOW METALS, NF, EP, BP, JPE, CHP (S-142)
01 1U.S.A
01 1Active
01 1Blank
Pfanstiehl, a global leader in the manufacture of cGMP high purity, low endotoxin, low metals (HPLE-LM)TM injectable grade excipients.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 41241
Submission : 2025-01-28
Status : Active
Type : IV
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PharmaCompass offers a list of Succinic 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 Succinic Acid manufacturer or Succinic Acid supplier for your needs.
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PharmaCompass also assists you with knowing the Succinic Acid API Price utilized in the formulation of products. Succinic Acid API Price is not always fixed or binding as the Succinic Acid Price is obtained through a variety of data sources. The Succinic Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A DSSTox_CID_3602 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DSSTox_CID_3602, including repackagers and relabelers. The FDA regulates DSSTox_CID_3602 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DSSTox_CID_3602 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A DSSTox_CID_3602 supplier is an individual or a company that provides DSSTox_CID_3602 active pharmaceutical ingredient (API) or DSSTox_CID_3602 finished formulations upon request. The DSSTox_CID_3602 suppliers may include DSSTox_CID_3602 API manufacturers, exporters, distributors and traders.
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A DSSTox_CID_3602 DMF (Drug Master File) is a document detailing the whole manufacturing process of DSSTox_CID_3602 active pharmaceutical ingredient (API) in detail. Different forms of DSSTox_CID_3602 DMFs exist exist since differing nations have different regulations, such as DSSTox_CID_3602 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A DSSTox_CID_3602 DMF submitted to regulatory agencies in the US is known as a USDMF. DSSTox_CID_3602 USDMF includes data on DSSTox_CID_3602's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The DSSTox_CID_3602 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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