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General MedicationsORALGeneric

STAVUDINE; LAMIVUDINE; NEVIRAPINE

STAVUDINE; LAMIVUDINE; NEVIRAPINE

Standard Dose
40MG; 150MG; 200MG
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: None (Tentative Approval)
Summary

Approval overview STAVUDINE; LAMIVUDINE; NEVIRAPINE is listed in Drugs@FDA under application 022346 (NDA).

Review priority: STANDARD Marketing status: None (Tentative Approval) Active ingredient STAVUDINE; LAMIVUDINE; NEVIRAPINE Form and strength TABLET; ORAL - 40MG; 150MG; 200MG Sponsor PHARMACARE LTD Submission history Latest submission status date: 2009-02-27 00:00:00.

Structured Monograph

Clinical summary

Approval overview STAVUDINE; LAMIVUDINE; NEVIRAPINE is listed in Drugs@FDA under application 022346 (NDA). Review priority: STANDARD Marketing status: None (Tentative Approval) Active ingredient STAVUDINE; LAMIVUDINE; NEVIRAPINE Form and strength TABLET; ORAL - 40MG; 150MG; 200MG Sponsor PHARMACARE LTD Submission history Latest submission status date: 2009-02-27 00:00:00. Submission type: ORIG.

Monitoring

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

Interaction Notes

  • No interaction notes stored yet.
STAVUDINE; LAMIVUDINE; NEVIRAPINE (STAVUDINE; LAMIVUDINE; NEVIRAPINE) | Drug Monograph | MedicHelpline