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GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 26257
Submission : 2012-08-12
Status : Active
Type : II
A Entecavir Intermediate VIII Isomer manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Entecavir Intermediate VIII Isomer, including repackagers and relabelers. The FDA regulates Entecavir Intermediate VIII Isomer manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Entecavir Intermediate VIII Isomer 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 Entecavir Intermediate VIII Isomer supplier is an individual or a company that provides Entecavir Intermediate VIII Isomer active pharmaceutical ingredient (API) or Entecavir Intermediate VIII Isomer finished formulations upon request. The Entecavir Intermediate VIII Isomer suppliers may include Entecavir Intermediate VIII Isomer API manufacturers, exporters, distributors and traders.
click here to find a list of Entecavir Intermediate VIII Isomer suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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