# PHYTONADIONE

NDC: 43066-132
Generic name: PHYTONADIONE
Labeler / Manufacturer: Baxter Healthcare Corporation
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, EMULSION
Routes: INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Marketing started: 20260226

FDA application: ANDA216852

## Active ingredients

- PHYTONADIONE: 1 mg/.5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43066-132"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43066-132
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=98fa1675-8af1-42c5-bbab-8b3632d52a0f