01 13M Drug Delivery Systems
01 1CI-1017 TRANSDERMAL DELIVERY SYSTEM
01 1U.S.A
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 14318
Submission : 1999-07-28
Status : Inactive
Type : II
A Ci-1017 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ci-1017, including repackagers and relabelers. The FDA regulates Ci-1017 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ci-1017 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 Ci-1017 supplier is an individual or a company that provides Ci-1017 active pharmaceutical ingredient (API) or Ci-1017 finished formulations upon request. The Ci-1017 suppliers may include Ci-1017 API manufacturers, exporters, distributors and traders.
click here to find a list of Ci-1017 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Ci-1017 DMF (Drug Master File) is a document detailing the whole manufacturing process of Ci-1017 active pharmaceutical ingredient (API) in detail. Different forms of Ci-1017 DMFs exist exist since differing nations have different regulations, such as Ci-1017 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Ci-1017 DMF submitted to regulatory agencies in the US is known as a USDMF. Ci-1017 USDMF includes data on Ci-1017's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Ci-1017 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Ci-1017 suppliers with USDMF on PharmaCompass.
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