United States · FDA National Drug Code directory
Phytonadione
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 65219-635_02a39690-38e6-42e9-9897-391c2df9e07e
- Product NDC
- 65219-635
- Form
- INJECTION, EMULSION
- Composition / generic term
- Phytonadione
- Labeler
- Fresenius Kabi USA, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250510
- Source listing expiry
- 20261231
Source-listed ingredients
- PHYTONADIONE — 10 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 2 TRAY in 1 CARTON (65219-635-01) / 5 VIAL, SINGLE-DOSE in 1 TRAY (65219-635-00) / 1 mL in 1 VIAL, SINGLE-DOSE · 65219-635-01
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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