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General MedicationsORALGeneric

TARGINIQ

NALOXONE HYDROCHLORIDE; OXYCODONE HYDROCHLORIDE

Standard Dose
20MG;40MG
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: Discontinued
Summary

Approval overview TARGINIQ is listed in Drugs@FDA under application 205777 (NDA).

Review priority: STANDARD Marketing status: Discontinued Active ingredient NALOXONE HYDROCHLORIDE; OXYCODONE HYDROCHLORIDE Form and strength TABLET, EXTENDED RELEASE;ORAL - 20MG;40MG Sponsor PURDUE PHARMA LP Submission history Latest submission status date: 2018-09-18 00:00:00.

Structured Monograph

Clinical summary

Approval overview TARGINIQ is listed in Drugs@FDA under application 205777 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient NALOXONE HYDROCHLORIDE; OXYCODONE HYDROCHLORIDE Form and strength TABLET, EXTENDED RELEASE;ORAL - 20MG;40MG Sponsor PURDUE PHARMA LP Submission history Latest submission status date: 2018-09-18 00:00:00. Submission type: SUPPL.

Monitoring

  • • Marketing status: Discontinued
  • • Review priority: STANDARD

Interaction Notes

  • No interaction notes stored yet.