# Octreotide Acetate

NDC: 0480-9259
Generic name: Octreotide Acetate
Labeler / Manufacturer: Teva Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: KIT
Routes: INTRAMUSCULAR
Marketing started: 20241001

FDA application: ANDA210317

## Active ingredients

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## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0480-9259"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0480-9259
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d9739ea6-74de-4a41-a806-6e827a23cedb