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General MedicationsORALGeneric

OXYCODONE HYDROCHLORIDE

OXYCODONE HYDROCHLORIDE

Standard Dose
40MG
Max Dose
Refer to approved labeling
Primary Use
Marketing status: None (Tentative Approval)
Summary

Approval overview OXYCODONE HYDROCHLORIDE is listed in Drugs@FDA under application 077822 (ANDA).

Marketing status: None (Tentative Approval) Active ingredient OXYCODONE HYDROCHLORIDE Form and strength TABLET, EXTENDED RELEASE; ORAL - 40MG Sponsor MALLINCKRODT Submission history Latest submission status date: 2008-07-24 00:00:00.

Structured Monograph

Clinical summary

Approval overview OXYCODONE HYDROCHLORIDE is listed in Drugs@FDA under application 077822 (ANDA). Marketing status: None (Tentative Approval) Active ingredient OXYCODONE HYDROCHLORIDE Form and strength TABLET, EXTENDED RELEASE; ORAL - 40MG Sponsor MALLINCKRODT Submission history Latest submission status date: 2008-07-24 00:00:00. Submission type: ORIG.

Monitoring

  • • Review priority: STANDARD
  • • Marketing status: None (Tentative Approval)

Interaction Notes

  • No interaction notes stored yet.
OXYCODONE HYDROCHLORIDE (OXYCODONE HYDROCHLORIDE) | Drug Monograph | MedicHelpline