# PHYTONADIONE

NDC: 70095-154
Generic name: Phytonadione
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, EMULSION
Routes: INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Marketing started: 20260610

FDA application: ANDA216298

## 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:"70095-154"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70095-154
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=51c175dd-02f9-68d1-e063-6294a90a4b36