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01 1RP SCHERER GMBH & CO. KG
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01 1OXYPHENBUTAZONE CAPSULE 100MG
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01 1Germany
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01 1Inactive
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01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 1924
Submission : 1972-05-01
Status : Inactive
Type : II
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PharmaCompass offers a list of Oxyphenbutazone 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 Oxyphenbutazone manufacturer or Oxyphenbutazone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Oxyphenbutazone manufacturer or Oxyphenbutazone supplier.
PharmaCompass also assists you with knowing the Oxyphenbutazone API Price utilized in the formulation of products. Oxyphenbutazone API Price is not always fixed or binding as the Oxyphenbutazone Price is obtained through a variety of data sources. The Oxyphenbutazone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Telidal manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Telidal, including repackagers and relabelers. The FDA regulates Telidal manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Telidal API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Telidal supplier is an individual or a company that provides Telidal active pharmaceutical ingredient (API) or Telidal finished formulations upon request. The Telidal suppliers may include Telidal API manufacturers, exporters, distributors and traders.
click here to find a list of Telidal suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Telidal DMF (Drug Master File) is a document detailing the whole manufacturing process of Telidal active pharmaceutical ingredient (API) in detail. Different forms of Telidal DMFs exist exist since differing nations have different regulations, such as Telidal USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Telidal DMF submitted to regulatory agencies in the US is known as a USDMF. Telidal USDMF includes data on Telidal's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Telidal USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Telidal suppliers with USDMF on PharmaCompass.
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