01 1BASF
01 1POLOXALENE USP
01 1Germany
01 1Active
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 18382
Submission : 2005-05-27
Status : Active
Type : II
33
PharmaCompass offers a list of Detalan 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 Detalan manufacturer or Detalan supplier for your needs.
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A Pluronic F 127 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pluronic F 127, including repackagers and relabelers. The FDA regulates Pluronic F 127 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pluronic F 127 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 Pluronic F 127 supplier is an individual or a company that provides Pluronic F 127 active pharmaceutical ingredient (API) or Pluronic F 127 finished formulations upon request. The Pluronic F 127 suppliers may include Pluronic F 127 API manufacturers, exporters, distributors and traders.
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A Pluronic F 127 DMF (Drug Master File) is a document detailing the whole manufacturing process of Pluronic F 127 active pharmaceutical ingredient (API) in detail. Different forms of Pluronic F 127 DMFs exist exist since differing nations have different regulations, such as Pluronic F 127 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Pluronic F 127 DMF submitted to regulatory agencies in the US is known as a USDMF. Pluronic F 127 USDMF includes data on Pluronic F 127's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Pluronic F 127 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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