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
- 81607-020_1a12da69-249c-42d2-8cde-1f0ecfbc299c
- Product NDC
- 81607-020
- Form
- INJECTION, EMULSION
- Composition / generic term
- Phytonadione
- Labeler
- Orbicular Pharmaceutical Technologies Private Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260324
- Source listing expiry
- 20271231
Source-listed ingredients
- PHYTONADIONE — 1 mg/.5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 CARTON in 1 CARTON (81607-020-02) / 1 BLISTER PACK in 1 CARTON (81607-020-01) / 1 SYRINGE in 1 BLISTER PACK / .5 mL in 1 SYRINGE · 81607-020-02
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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