FDA NDC Directory · JSON-LD · Markdown

Phytonadione

NDC 65219-635 · HUMAN PRESCRIPTION DRUG · INJECTION, EMULSION

Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA219212
Dosage form / routeINJECTION, EMULSION · INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
Active ingredientsPHYTONADIONE (10 mg/mL)
Marketing started20250510
Package count1

External sources

Source: openFDA. Public-domain (CC0).