United States · FDA National Drug Code directory

Fosaprepitant

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
72205-054_604e47a7-2f8f-40f8-9595-00b09be51e40
Product NDC
72205-054
Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Composition / generic term
Fosaprepitant
Labeler
Novadoz Pharmaceuticals LLC
Marketing category
ANDA
Marketing start / end (source format)
20200512
Source listing expiry
20261231

Source-listed ingredients

  • FOSAPREPITANT DIMEGLUMINE — 150 mg/5mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 VIAL, SINGLE-DOSE in 1 CARTON (72205-054-01) / 5 mL in 1 VIAL, SINGLE-DOSE · 72205-054-01

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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