United States · FDA National Drug Code directory

Foscarnet Sodium

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
25021-189_f5829ec8-15e6-43a4-a5f0-68ea0cddb8c8
Product NDC
25021-189
Form
INJECTION, SOLUTION
Composition / generic term
Foscarnet Sodium
Labeler
Sagent Pharmaceuticals
Marketing category
ANDA
Marketing start / end (source format)
20210515
Source listing expiry
20261231

Source-listed ingredients

  • FOSCARNET SODIUM — 24 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 10 BAG in 1 CARTON (25021-189-84) / 250 mL in 1 BAG · 25021-189-84

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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