01 1Daicel Corporation
01 1N-{1-(S)-ETHOXYCARBONYL-3-PHENYLPROPYL}-(S)-ALANINE
01 1Japan
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9393
Submission : 1991-10-18
Status : Inactive
Type : II
19
PharmaCompass offers a list of Surecn1221172 API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Surecn1221172 manufacturer or Surecn1221172 supplier for your needs.
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A Surecn1221172 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Surecn1221172, including repackagers and relabelers. The FDA regulates Surecn1221172 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Surecn1221172 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Surecn1221172 supplier is an individual or a company that provides Surecn1221172 active pharmaceutical ingredient (API) or Surecn1221172 finished formulations upon request. The Surecn1221172 suppliers may include Surecn1221172 API manufacturers, exporters, distributors and traders.
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A Surecn1221172 DMF (Drug Master File) is a document detailing the whole manufacturing process of Surecn1221172 active pharmaceutical ingredient (API) in detail. Different forms of Surecn1221172 DMFs exist exist since differing nations have different regulations, such as Surecn1221172 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Surecn1221172 DMF submitted to regulatory agencies in the US is known as a USDMF. Surecn1221172 USDMF includes data on Surecn1221172's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Surecn1221172 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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