0078-0182Level 3
Sandostatin (octreotide acetate)
**Product type:** Human Prescription Drug
**Active ingredient:** OCTREOTIDE ACETATE
**Strength:** 500 ug/mL
**Dosage form:** Injection, Solution
**Route:** Intravenous; Subcutaneous
**Labeler:** Novartis Pharmaceuticals Corporation
**Marketing category:** NDA (NDA019667)
**Pharmacologic class:** Somatostatin Analog [EPC], Somatostatin Receptor Agonists [MoA]
GET
/api/v1/systems/ndc_fda/nodes/0078-0182Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.