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CardiovascularINJECTIONGeneric

SANDOSTATIN

OCTREOTIDE ACETATE

Standard Dose
EQ 0.2MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: Discontinued
Summary

Approval overview SANDOSTATIN is listed in Drugs@FDA under application 019667 (NDA).

Review priority: STANDARD Marketing status: Discontinued Active ingredient OCTREOTIDE ACETATE Form and strength INJECTABLE;INJECTION - EQ 0.2MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor NOVARTIS Submission history Latest submission status date: 2024-07-11 00:00:00.

Structured Monograph

Clinical summary

Approval overview SANDOSTATIN is listed in Drugs@FDA under application 019667 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient OCTREOTIDE ACETATE Form and strength INJECTABLE;INJECTION - EQ 0.2MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor NOVARTIS Submission history Latest submission status date: 2024-07-11 00:00:00. Submission type: SUPPL.

Monitoring

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

Interaction Notes

  • No interaction notes stored yet.
SANDOSTATIN (OCTREOTIDE ACETATE) | Drug Monograph | MedicHelpline