01 1Olon S.p.A
01 1PAROMOMYCIN SULFATE
01 1Italy
01 1Active
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13576
Submission : 1998-09-01
Status : Active
Type : II
31
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A Aminosidin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aminosidin, including repackagers and relabelers. The FDA regulates Aminosidin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aminosidin 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 Aminosidin supplier is an individual or a company that provides Aminosidin active pharmaceutical ingredient (API) or Aminosidin finished formulations upon request. The Aminosidin suppliers may include Aminosidin API manufacturers, exporters, distributors and traders.
click here to find a list of Aminosidin suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Aminosidin DMF (Drug Master File) is a document detailing the whole manufacturing process of Aminosidin active pharmaceutical ingredient (API) in detail. Different forms of Aminosidin DMFs exist exist since differing nations have different regulations, such as Aminosidin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Aminosidin DMF submitted to regulatory agencies in the US is known as a USDMF. Aminosidin USDMF includes data on Aminosidin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Aminosidin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Aminosidin suppliers with USDMF on PharmaCompass.
