01 1ANUS LABORATORIES LTD
01 1CIS (+) HYDROXY LACTAM
01 1India
01 1Active
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 23168
Submission : 2009-10-06
Status : Active
Type : II
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PharmaCompass offers a list of Moxalactam 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 Moxalactam manufacturer or Moxalactam supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Moxalactam manufacturer or Moxalactam supplier.
PharmaCompass also assists you with knowing the Moxalactam API Price utilized in the formulation of products. Moxalactam API Price is not always fixed or binding as the Moxalactam Price is obtained through a variety of data sources. The Moxalactam Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Shiomarin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Shiomarin, including repackagers and relabelers. The FDA regulates Shiomarin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Shiomarin 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 Shiomarin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Shiomarin supplier is an individual or a company that provides Shiomarin active pharmaceutical ingredient (API) or Shiomarin finished formulations upon request. The Shiomarin suppliers may include Shiomarin API manufacturers, exporters, distributors and traders.
click here to find a list of Shiomarin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Shiomarin DMF (Drug Master File) is a document detailing the whole manufacturing process of Shiomarin active pharmaceutical ingredient (API) in detail. Different forms of Shiomarin DMFs exist exist since differing nations have different regulations, such as Shiomarin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Shiomarin DMF submitted to regulatory agencies in the US is known as a USDMF. Shiomarin USDMF includes data on Shiomarin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Shiomarin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Shiomarin suppliers with USDMF on PharmaCompass.
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