01 1Olon S.p.A
02 1Sandoz B2B
01 1TENIPOSIDE
02 1TENIPOSIDE (VM 26)
01 1Italy
02 1Switzerland
01 1Active
02 1Inactive
01 2Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16845
Submission : 2003-10-10
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4044
Submission : 1980-12-05
Status : Inactive
Type : II
A Teniposide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Teniposide, including repackagers and relabelers. The FDA regulates Teniposide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Teniposide 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 Teniposide supplier is an individual or a company that provides Teniposide active pharmaceutical ingredient (API) or Teniposide finished formulations upon request. The Teniposide suppliers may include Teniposide API manufacturers, exporters, distributors and traders.
click here to find a list of Teniposide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Teniposide DMF (Drug Master File) is a document detailing the whole manufacturing process of Teniposide active pharmaceutical ingredient (API) in detail. Different forms of Teniposide DMFs exist exist since differing nations have different regulations, such as Teniposide USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Teniposide DMF submitted to regulatory agencies in the US is known as a USDMF. Teniposide USDMF includes data on Teniposide's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Teniposide USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Teniposide suppliers with USDMF on PharmaCompass.
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