# Oxytocin

NDC: 63323-012
Generic name: OXYTOCIN
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20000810

FDA application: NDA018248

## Active ingredients

- OXYTOCIN: 10 [USP'U]/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63323-012"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63323-012
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6d7d1280-f286-4f39-89f3-2b96571810e6