01 1FDC
01 1CINNARIZINE
01 1India
01 1Active
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 31934
Submission : 2017-09-07
Status : Active
Type : II
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PharmaCompass offers a list of Cinnarizine 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 Cinnarizine manufacturer or Cinnarizine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cinnarizine manufacturer or Cinnarizine supplier.
PharmaCompass also assists you with knowing the Cinnarizine API Price utilized in the formulation of products. Cinnarizine API Price is not always fixed or binding as the Cinnarizine Price is obtained through a variety of data sources. The Cinnarizine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lazeta manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lazeta, including repackagers and relabelers. The FDA regulates Lazeta manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lazeta 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 Lazeta manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lazeta supplier is an individual or a company that provides Lazeta active pharmaceutical ingredient (API) or Lazeta finished formulations upon request. The Lazeta suppliers may include Lazeta API manufacturers, exporters, distributors and traders.
click here to find a list of Lazeta suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Lazeta DMF (Drug Master File) is a document detailing the whole manufacturing process of Lazeta active pharmaceutical ingredient (API) in detail. Different forms of Lazeta DMFs exist exist since differing nations have different regulations, such as Lazeta USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Lazeta DMF submitted to regulatory agencies in the US is known as a USDMF. Lazeta USDMF includes data on Lazeta's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Lazeta USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Lazeta suppliers with USDMF on PharmaCompass.
