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02 1Unipex
03 1Viatris
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01 1France
02 3U.S.A
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02 1Inactive
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01 165392-3101
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GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19093
Submission : 2006-01-06
Status : Active
Type : II
NDC Package Code : 65392-3101
Start Marketing Date : 2006-10-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (55kg/55kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 23409
Submission : 2009-12-29
Status : Inactive
Type : II
NDC Package Code : 65392-3102
Start Marketing Date : 2006-10-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (55kg/55kg)
Marketing Category : BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
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A Vorinostat,SAHA,Zolinza,MK-0683 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vorinostat,SAHA,Zolinza,MK-0683, including repackagers and relabelers. The FDA regulates Vorinostat,SAHA,Zolinza,MK-0683 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vorinostat,SAHA,Zolinza,MK-0683 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Vorinostat,SAHA,Zolinza,MK-0683 supplier is an individual or a company that provides Vorinostat,SAHA,Zolinza,MK-0683 active pharmaceutical ingredient (API) or Vorinostat,SAHA,Zolinza,MK-0683 finished formulations upon request. The Vorinostat,SAHA,Zolinza,MK-0683 suppliers may include Vorinostat,SAHA,Zolinza,MK-0683 API manufacturers, exporters, distributors and traders.
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