01 1EASTMAN KODAK
02 1SAFC
01 2RHODAMINE 123
01 2U.S.A
01 2Inactive
01 2Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7749
Submission : 1988-11-08
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13047
Submission : 1998-06-28
Status : Inactive
Type : II
A Rhodamine 123 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Rhodamine 123, including repackagers and relabelers. The FDA regulates Rhodamine 123 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Rhodamine 123 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 Rhodamine 123 supplier is an individual or a company that provides Rhodamine 123 active pharmaceutical ingredient (API) or Rhodamine 123 finished formulations upon request. The Rhodamine 123 suppliers may include Rhodamine 123 API manufacturers, exporters, distributors and traders.
click here to find a list of Rhodamine 123 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Rhodamine 123 DMF (Drug Master File) is a document detailing the whole manufacturing process of Rhodamine 123 active pharmaceutical ingredient (API) in detail. Different forms of Rhodamine 123 DMFs exist exist since differing nations have different regulations, such as Rhodamine 123 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Rhodamine 123 DMF submitted to regulatory agencies in the US is known as a USDMF. Rhodamine 123 USDMF includes data on Rhodamine 123's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Rhodamine 123 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Rhodamine 123 suppliers with USDMF on PharmaCompass.
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