# Phytonadione

NDC: 65219-635
Generic name: Phytonadione
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, EMULSION
Routes: INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Marketing started: 20250510

FDA application: ANDA219212

## Active ingredients

- PHYTONADIONE: 10 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65219-635"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65219-635
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=02a39690-38e6-42e9-9897-391c2df9e07e