NDC 67457-239
Octreotide Acetate 50 ug per 1 mL injection, solution
On the label: Mylan Institutional LLC.
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 Mylan Institutional LLC names for other drugs.
Recalls
- Oct 7, 2022 · Class I · Viatris Inc
Presence of Particulate Matter: Product complaint for the presence of glass particles in a syringe.
Lots: Lot #: AJ21002, Exp. 03/2024
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Octreotide: every company that makes it
- Form
- injection, solution, intravenous; subcutaneous
- Strength
- 50 ug per 1 mL
- Approval
- ANDA ANDA079198
- On the market since
- Apr 1, 2011
- Package NDCs
67457-239-0067457-239-01- Official label
- DailyMed (National Library of Medicine), updated Jul 15, 2024
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