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01 1Johnson & Johnson Innovative Medicine
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01 1LEVOCABASTINE HCL.(BULK)
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01 1U.S.A
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01 1Inactive
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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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PharmaCompass offers a list of Levocabastine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Levocabastine manufacturer or Levocabastine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Levocabastine manufacturer or Levocabastine supplier.
PharmaCompass also assists you with knowing the Levocabastine API Price utilized in the formulation of products. Levocabastine API Price is not always fixed or binding as the Levocabastine Price is obtained through a variety of data sources. The Levocabastine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A livostin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of livostin, including repackagers and relabelers. The FDA regulates livostin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. livostin 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 livostin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A livostin supplier is an individual or a company that provides livostin active pharmaceutical ingredient (API) or livostin finished formulations upon request. The livostin suppliers may include livostin API manufacturers, exporters, distributors and traders.
click here to find a list of livostin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A livostin DMF (Drug Master File) is a document detailing the whole manufacturing process of livostin active pharmaceutical ingredient (API) in detail. Different forms of livostin DMFs exist exist since differing nations have different regulations, such as livostin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A livostin DMF submitted to regulatory agencies in the US is known as a USDMF. livostin USDMF includes data on livostin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The livostin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of livostin suppliers with USDMF on PharmaCompass.
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