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
72603-450_243a7c82-4e3c-43b7-a6bb-c305d48c9f61
Product NDC
72603-450
Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Composition / generic term
Fosaprepitant
Labeler
Northstar Rx LLC
Marketing category
ANDA
Marketing start / end (source format)
20190905
Source listing expiry
20271231

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 (72603-450-01) / 5 mL in 1 VIAL, SINGLE-DOSE · 72603-450-01

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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