01 2Jiangsu Yuexing Pharmaceutical Co., Ltd
01 17 AMINO DESACETOXY CEPHALOSPORANIC ACID (7 ADCA)
02 1NATURAL AND ARTIFICIAL MIXED FRUIT FLVP FT 1789
01 2China
01 2Active
01 2Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 31864
Submission : 2017-06-20
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 31684
Submission : 2017-04-07
Status : Active
Type : IV
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PharmaCompass offers a list of Cefalexine Ep Impurity B 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 Cefalexine Ep Impurity B manufacturer or Cefalexine Ep Impurity B supplier for your needs.
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PharmaCompass also assists you with knowing the Cefalexine Ep Impurity B API Price utilized in the formulation of products. Cefalexine Ep Impurity B API Price is not always fixed or binding as the Cefalexine Ep Impurity B Price is obtained through a variety of data sources. The Cefalexine Ep Impurity B Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cefalexine Ep Impurity B manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cefalexine Ep Impurity B, including repackagers and relabelers. The FDA regulates Cefalexine Ep Impurity B manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cefalexine Ep Impurity B 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 Cefalexine Ep Impurity B supplier is an individual or a company that provides Cefalexine Ep Impurity B active pharmaceutical ingredient (API) or Cefalexine Ep Impurity B finished formulations upon request. The Cefalexine Ep Impurity B suppliers may include Cefalexine Ep Impurity B API manufacturers, exporters, distributors and traders.
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A Cefalexine Ep Impurity B DMF (Drug Master File) is a document detailing the whole manufacturing process of Cefalexine Ep Impurity B active pharmaceutical ingredient (API) in detail. Different forms of Cefalexine Ep Impurity B DMFs exist exist since differing nations have different regulations, such as Cefalexine Ep Impurity B USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Cefalexine Ep Impurity B DMF submitted to regulatory agencies in the US is known as a USDMF. Cefalexine Ep Impurity B USDMF includes data on Cefalexine Ep Impurity B's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Cefalexine Ep Impurity B USDMF is kept confidential to protect the manufacturer’s intellectual property.
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