01 1Cyalume Specialty Products
01 1GLUCOSAPURE (GLUCOSAMINE SULFATE)
01 1U.S.A
01 1Active
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 14915
Submission : 2000-06-08
Status : Active
Type : II
A Glucosamine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Glucosamine, including repackagers and relabelers. The FDA regulates Glucosamine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Glucosamine 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 Glucosamine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Glucosamine supplier is an individual or a company that provides Glucosamine active pharmaceutical ingredient (API) or Glucosamine finished formulations upon request. The Glucosamine suppliers may include Glucosamine API manufacturers, exporters, distributors and traders.
click here to find a list of Glucosamine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Glucosamine DMF (Drug Master File) is a document detailing the whole manufacturing process of Glucosamine active pharmaceutical ingredient (API) in detail. Different forms of Glucosamine DMFs exist exist since differing nations have different regulations, such as Glucosamine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Glucosamine DMF submitted to regulatory agencies in the US is known as a USDMF. Glucosamine USDMF includes data on Glucosamine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Glucosamine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Glucosamine suppliers with USDMF on PharmaCompass.
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