01 1Cyalume Specialty Products
01 1DICHLORALPHENAZONE USP
01 1U.S.A
01 1Active
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 23691
Submission : 2010-04-06
Status : Active
Type : II
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A 480-30-8 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 480-30-8, including repackagers and relabelers. The FDA regulates 480-30-8 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 480-30-8 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 480-30-8 supplier is an individual or a company that provides 480-30-8 active pharmaceutical ingredient (API) or 480-30-8 finished formulations upon request. The 480-30-8 suppliers may include 480-30-8 API manufacturers, exporters, distributors and traders.
click here to find a list of 480-30-8 suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A 480-30-8 DMF (Drug Master File) is a document detailing the whole manufacturing process of 480-30-8 active pharmaceutical ingredient (API) in detail. Different forms of 480-30-8 DMFs exist exist since differing nations have different regulations, such as 480-30-8 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A 480-30-8 DMF submitted to regulatory agencies in the US is known as a USDMF. 480-30-8 USDMF includes data on 480-30-8's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 480-30-8 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of 480-30-8 suppliers with USDMF on PharmaCompass.
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