NDC 0078-0180
Sandostatin 50 ug per 1 mL injection, solution
On the label: Novartis Pharmaceuticals Corporation.
Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Novartis Pharmaceuticals Corporation names for other drugs.
Product details
- Generic drug
- Octreotide: every company that makes it
- Form
- injection, solution, intravenous; subcutaneous
- Strength
- 50 ug per 1 mL
- Approval
- NDA NDA019667
- On the market since
- Oct 21, 1988
- Package NDCs
0078-0180-010078-0180-61- Official label
- DailyMed (National Library of Medicine), updated Jul 22, 2026
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