NDC 0480-9259

Octreotide Acetate 3.33 mg per 1 mL kit

On the label: Teva Pharmaceuticals, 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 Teva Pharmaceuticals, Inc. names for other drugs.

Recalls

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
kit, intramuscular
Strength
3.33 mg per 1 mL
Approval
ANDA ANDA210317
On the market since
Oct 1, 2024
Package NDCs
0480-9258-01 0480-9259-08 0480-9263-21
Official label
DailyMed (National Library of Medicine), updated Jul 30, 2024

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