01 1Zhejiang Medicine Co Ltd
01 1MIGLITOL
01 1China
01 1Active
01 1Complete
GDUFA
DMF Review : Complete
Rev. Date : 2013-01-08
Pay. Date : 2012-12-23
DMF Number : 18833
Submission : 2005-01-22
Status : Active
Type : II
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PharmaCompass offers a list of Miglitol 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 Miglitol manufacturer or Miglitol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Miglitol manufacturer or Miglitol supplier.
PharmaCompass also assists you with knowing the Miglitol API Price utilized in the formulation of products. Miglitol API Price is not always fixed or binding as the Miglitol Price is obtained through a variety of data sources. The Miglitol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Glyset manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Glyset, including repackagers and relabelers. The FDA regulates Glyset manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Glyset 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 Glyset manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Glyset supplier is an individual or a company that provides Glyset active pharmaceutical ingredient (API) or Glyset finished formulations upon request. The Glyset suppliers may include Glyset API manufacturers, exporters, distributors and traders.
click here to find a list of Glyset suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Glyset DMF (Drug Master File) is a document detailing the whole manufacturing process of Glyset active pharmaceutical ingredient (API) in detail. Different forms of Glyset DMFs exist exist since differing nations have different regulations, such as Glyset USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Glyset DMF submitted to regulatory agencies in the US is known as a USDMF. Glyset USDMF includes data on Glyset's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Glyset USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Glyset suppliers with USDMF on PharmaCompass.
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