NDC 0641-6174
Octreotide Acetate 50 ug per 1 mL injection, solution
On the label: Hikma Pharmaceuticals USA Inc..
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 Hikma Pharmaceuticals USA Inc. 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
- ANDA ANDA076313
- On the market since
- Apr 4, 2005
- Package NDCs
0641-6174-010641-6174-10- Official label
- DailyMed (National Library of Medicine), updated Jan 13, 2026
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