01 1ALP Pharm
01 1SULPIRIDE EP
01 1China
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 20209
Submission : 2007-01-05
Status : Inactive
Type : II
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A Levopraid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Levopraid, including repackagers and relabelers. The FDA regulates Levopraid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Levopraid 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 Levopraid manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Levopraid supplier is an individual or a company that provides Levopraid active pharmaceutical ingredient (API) or Levopraid finished formulations upon request. The Levopraid suppliers may include Levopraid API manufacturers, exporters, distributors and traders.
click here to find a list of Levopraid suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Levopraid DMF (Drug Master File) is a document detailing the whole manufacturing process of Levopraid active pharmaceutical ingredient (API) in detail. Different forms of Levopraid DMFs exist exist since differing nations have different regulations, such as Levopraid USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Levopraid DMF submitted to regulatory agencies in the US is known as a USDMF. Levopraid USDMF includes data on Levopraid's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Levopraid USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Levopraid suppliers with USDMF on PharmaCompass.
