Mydayis

Active Ingredient(s): Mixed Salts of a Single-Entity Amphetamine
FDA Approved: * June 20, 2017
Pharm Company: * SHIRE DEV LLC
Category: ADD / ADHD

* This drug may consist of multiple approval dates, manufacturers, or distributors. If applicable, they would be listed below under "NDC Database Records".



Mydayis Overview

Amphetamine[note 1] (contracted from alphamethylphenethylamine) is a potent central nervous system (CNS) stimulant that is used in the treatment of attention deficit hyperactivity disorder (ADHD), narcolepsy, and obesity. Amphetamine was discovered in 1887 and exists as two enantiomers:[note 2] levoamphetamine and dextroamphetamine. Amphetamine properly refers to a specific chemical, the racemic free base, which is equal parts of the two enantiomers, levoamphetamine and dextroamphetamine, in ...

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Details May Include Instructions, Side Effects, Interactions, Etc. Drug monograph is from Wikipedia. All text is available under the terms of the GFDL (GNU Free Documentation License). Source: en.wikipedia.org/wiki/Amphetamine

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Possible Dosages for this and Related Drugs:

Mixed Salts of a Single-Entity Amphetamine
  • Capsule, Extended Release: 12.5mg, 25mg, 37.5mg, 50mg
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

NDC Database Records for Mydayis: (4 results)

Sorted by National Drug Code
  • 54092-468 Mydayis Oral Capsule, Extended Release by Shire Us Manufacturing Inc.
  • 54092-471 Mydayis Oral Capsule, Extended Release by Shire Us Manufacturing Inc.
  • 54092-474 Mydayis Oral Capsule, Extended Release by Shire Us Manufacturing Inc.
  • 54092-477 Mydayis Oral Capsule, Extended Release by Shire Us Manufacturing Inc.



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