01 1Lupin Ltd
02 1Meiji Seika Pharma
03 1Orchid Pharma
04 1Sun Pharmaceutical Industries Limited
05 1ZHEJIANG HUAFANG PHARMACEUTICAL CO LTD
01 3CEFDITOREN PIVOXIL
02 2CEFDITOREN PIVOXIL DRUG SUBSTANCE
01 1China
02 3India
03 1Japan
01 2Active
02 3Inactive
01 5Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 23544
Submission : 2010-04-15
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17482
Submission : 2004-06-22
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 20292
Submission : 2007-02-22
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19011
Submission : 2005-12-07
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 25086
Submission : 2011-06-12
Status : Active
Type : II
77
PharmaCompass offers a list of Cefditoren Pivoxil 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 Cefditoren Pivoxil manufacturer or Cefditoren Pivoxil supplier for your needs.
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PharmaCompass also assists you with knowing the Cefditoren Pivoxil API Price utilized in the formulation of products. Cefditoren Pivoxil API Price is not always fixed or binding as the Cefditoren Pivoxil Price is obtained through a variety of data sources. The Cefditoren Pivoxil Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Meiact (TN) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Meiact (TN), including repackagers and relabelers. The FDA regulates Meiact (TN) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Meiact (TN) 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 Meiact (TN) manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Meiact (TN) supplier is an individual or a company that provides Meiact (TN) active pharmaceutical ingredient (API) or Meiact (TN) finished formulations upon request. The Meiact (TN) suppliers may include Meiact (TN) API manufacturers, exporters, distributors and traders.
click here to find a list of Meiact (TN) suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Meiact (TN) DMF (Drug Master File) is a document detailing the whole manufacturing process of Meiact (TN) active pharmaceutical ingredient (API) in detail. Different forms of Meiact (TN) DMFs exist exist since differing nations have different regulations, such as Meiact (TN) USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Meiact (TN) DMF submitted to regulatory agencies in the US is known as a USDMF. Meiact (TN) USDMF includes data on Meiact (TN)'s chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Meiact (TN) USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Meiact (TN) suppliers with USDMF on PharmaCompass.
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