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
69097-708_b3dd9cac-1295-48b6-b9b1-48d36cb732b9
Product NDC
69097-708
Form
INJECTION, EMULSION
Composition / generic term
Phytonadione
Labeler
Cipla USA Inc.
Marketing category
ANDA
Marketing start / end (source format)
20220427
Source listing expiry
20261231

Source-listed ingredients

  • PHYTONADIONE — 10 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 10 VIAL in 1 CARTON (69097-708-96) / 1 mL in 1 VIAL · 69097-708-96

Source and coverage

Open FDA National Drug Code directory

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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Phytonadione — United States | Molindra Medicines