01 1Hubei Biocause Heilen Pharmaceutical Co., Ltd
01 1HYOSCYAMINE SULFATE
01 1China
01 1Active
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 28614
Submission : 2014-09-02
Status : Active
Type : II
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A Levsin sulfate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Levsin sulfate, including repackagers and relabelers. The FDA regulates Levsin sulfate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Levsin sulfate 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 Levsin sulfate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Levsin sulfate supplier is an individual or a company that provides Levsin sulfate active pharmaceutical ingredient (API) or Levsin sulfate finished formulations upon request. The Levsin sulfate suppliers may include Levsin sulfate API manufacturers, exporters, distributors and traders.
click here to find a list of Levsin sulfate suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Levsin sulfate DMF (Drug Master File) is a document detailing the whole manufacturing process of Levsin sulfate active pharmaceutical ingredient (API) in detail. Different forms of Levsin sulfate DMFs exist exist since differing nations have different regulations, such as Levsin sulfate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Levsin sulfate DMF submitted to regulatory agencies in the US is known as a USDMF. Levsin sulfate USDMF includes data on Levsin sulfate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Levsin sulfate USDMF is kept confidential to protect the manufacturer’s intellectual property.
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