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
43598-671_aaffcc4e-88e7-4544-bedb-b508fddebd24
Product NDC
43598-671
Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Composition / generic term
Fosaprepitant
Labeler
Dr. Reddy's Laboratories Inc.,
Marketing category
ANDA
Marketing start / end (source format)
20260212
Source listing expiry
20271231

Source-listed ingredients

  • FOSAPREPITANT DIMEGLUMINE — 150 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 VIAL, SINGLE-DOSE in 1 CARTON (43598-671-11) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE · 43598-671-11

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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