Skip to main content
MedicHelpLine
Verified Professional Network190+ CountriesHIPAA-Aware Platform
Back to Drug Index
General MedicationsORALStandard

NALTREXONE HYDROCHLORIDE

NALTREXONE HYDROCHLORIDE

Standard Dose
100MG
Max Dose
Refer to approved labeling
Primary Use
Marketing status: Prescription
Summary

Approval overview NALTREXONE HYDROCHLORIDE is listed in Drugs@FDA under application 076264 (ANDA).

Marketing status: Prescription Active ingredient NALTREXONE HYDROCHLORIDE Form and strength TABLET;ORAL - 100MG Sponsor SPECGX LLC Submission history Latest submission status date: 2002-03-22 00:00:00.

Structured Monograph

Clinical summary

Approval overview NALTREXONE HYDROCHLORIDE is listed in Drugs@FDA under application 076264 (ANDA). Marketing status: Prescription Active ingredient NALTREXONE HYDROCHLORIDE Form and strength TABLET;ORAL - 100MG Sponsor SPECGX LLC Submission history Latest submission status date: 2002-03-22 00:00:00. Submission type: ORIG.

Monitoring

  • Marketing status: Prescription

Interaction Notes

  • No interaction notes stored yet.