United States · FDA National Drug Code directory

Ascorbic Acid

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
65219-027_d6fd1a37-70e1-477a-afc9-4977a54c7b75
Product NDC
65219-027
Form
INJECTION
Composition / generic term
Ascorbic Acid
Labeler
Fresenius Kabi USA, LLC
Marketing category
ANDA
Marketing start / end (source format)
20251208
Source listing expiry
20261231

Source-listed ingredients

  • ASCORBIC ACID — 500 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 25 VIAL, GLASS in 1 TRAY (65219-027-50) / 50 mL in 1 VIAL, GLASS (65219-027-05) · 65219-027-50
  • 1 VIAL, GLASS in 1 CARTON (65219-027-55) / 50 mL in 1 VIAL, GLASS · 65219-027-55

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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