01 1International Flavors and Fragrances
01 1MARINE COLLOIDS CARRAGEENAN
01 1U.S.A
01 1Active
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11678
Submission : 1995-09-13
Status : Active
Type : IV
A Carrageenan API manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Carrageenan API, including repackagers and relabelers. The FDA regulates Carrageenan API manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Carrageenan API 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 Carrageenan API supplier is an individual or a company that provides Carrageenan API active pharmaceutical ingredient (API) or Carrageenan API finished formulations upon request. The Carrageenan API suppliers may include Carrageenan API API manufacturers, exporters, distributors and traders.
click here to find a list of Carrageenan API suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Carrageenan API DMF (Drug Master File) is a document detailing the whole manufacturing process of Carrageenan API active pharmaceutical ingredient (API) in detail. Different forms of Carrageenan API DMFs exist exist since differing nations have different regulations, such as Carrageenan API USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Carrageenan API DMF submitted to regulatory agencies in the US is known as a USDMF. Carrageenan API USDMF includes data on Carrageenan API's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Carrageenan API USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Carrageenan API suppliers with USDMF on PharmaCompass.
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