Strength
200 ug/mL
Manufacturer
Sagent PharmaceuticalsNDC
25021046605
Classification
Generic
Dosage Form
INJECTION, SOLUTION
Route
INTRAVENOUS; SUBCUTANEOUS
Last Updated
4/22/2026
Active Ingredients
OCTREOTIDE ACETATEApproval Type
Generic (ANDA)
FDA Application
ANDA091041On Market Since
6/15/2023
Pharmacological Classes
Somatostatin Analog
Somatostatin Receptor Agonists
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