Application Information

This drug has been submitted to the FDA under the reference 076761/001.

Names and composition

"OXANDROLONE" is the commercial name of a drug composed of OXANDROLONE.

Forms

ApplId/ProductId Drug name Active ingredient Form Strenght
076761/001 OXANDROLONE OXANDROLONE TABLET/ORAL 2.5MG
076897/001 OXANDROLONE OXANDROLONE TABLET/ORAL 2.5MG
076897/002 OXANDROLONE OXANDROLONE TABLET/ORAL 10MG
077249/001 OXANDROLONE OXANDROLONE TABLET/ORAL 2.5MG
077249/002 OXANDROLONE OXANDROLONE TABLET/ORAL 10MG
077827/001 OXANDROLONE OXANDROLONE TABLET/ORAL 2.5MG
077827/002 OXANDROLONE OXANDROLONE TABLET/ORAL 10MG
078033/001 OXANDROLONE OXANDROLONE TABLET/ORAL 10MG

Similar Active Ingredient

ApplId/ProductId Drug name Active ingredient Form Strenght
013718/001 OXANDRIN OXANDROLONE TABLET/ORAL 2.5MG
013718/002 OXANDRIN OXANDROLONE TABLET/ORAL 10MG
076761/001 OXANDROLONE OXANDROLONE TABLET/ORAL 2.5MG
076897/001 OXANDROLONE OXANDROLONE TABLET/ORAL 2.5MG
076897/002 OXANDROLONE OXANDROLONE TABLET/ORAL 10MG
077249/001 OXANDROLONE OXANDROLONE TABLET/ORAL 2.5MG
077249/002 OXANDROLONE OXANDROLONE TABLET/ORAL 10MG
077827/001 OXANDROLONE OXANDROLONE TABLET/ORAL 2.5MG
077827/002 OXANDROLONE OXANDROLONE TABLET/ORAL 10MG
078033/001 OXANDROLONE OXANDROLONE TABLET/ORAL 10MG

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