US Drug Approval A040903

Imipramine Hydrochloride  Oct 24, 2012

3 approved drug products.
Imipramine Hydrochloride
  • Ingredients: Imipramine Hydrochloride;
  • Dosage form: tablet;
  • Route of administration: oral;
  • Strength: 10mg;
  • Approval date: October 24, 2012;
  • Marketing status: prescription.
Imipramine Hydrochloride
  • Ingredients: Imipramine Hydrochloride;
  • Dosage form: tablet;
  • Route of administration: oral;
  • Strength: 25mg;
  • Approval date: October 24, 2012;
  • Marketing status: prescription.
Imipramine Hydrochloride
  • Ingredients: Imipramine Hydrochloride;
  • Dosage form: tablet;
  • Route of administration: oral;
  • Strength: 50mg;
  • Approval date: October 24, 2012;
  • Marketing status: prescription.

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Source:  FDA Last updated:  Jul 8, 2019

From the Orange Book, a publication of the U.S. Food and Drug Administration. This record may not reflect the most current and accurate biomedical/scientific data available from the FDA.