01 1Johnson & Johnson Innovative Medicine
01 1LEVOCABASTINE HCL.(BULK)
01 1U.S.A
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5847
Submission : 1985-04-19
Status : Inactive
Type : II
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A levophta manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of levophta, including repackagers and relabelers. The FDA regulates levophta manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. levophta 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 levophta manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A levophta supplier is an individual or a company that provides levophta active pharmaceutical ingredient (API) or levophta finished formulations upon request. The levophta suppliers may include levophta API manufacturers, exporters, distributors and traders.
click here to find a list of levophta suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A levophta DMF (Drug Master File) is a document detailing the whole manufacturing process of levophta active pharmaceutical ingredient (API) in detail. Different forms of levophta DMFs exist exist since differing nations have different regulations, such as levophta USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A levophta DMF submitted to regulatory agencies in the US is known as a USDMF. levophta USDMF includes data on levophta's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The levophta USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of levophta suppliers with USDMF on PharmaCompass.
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