United States · FDA National Drug Code directory

Sodium Acetate

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
0409-3299_b7a713f4-3c97-484b-b182-2824e1e944bb
Product NDC
0409-3299
Form
INJECTION, SOLUTION, CONCENTRATE
Composition / generic term
sodium acetate
Labeler
Hospira, Inc.
Marketing category
NDA
Marketing start / end (source format)
20131119
Source listing expiry
20271231

Source-listed ingredients

  • SODIUM ACETATE ANHYDROUS — 164 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 25 VIAL in 1 CASE (0409-3299-25) / 100 mL in 1 VIAL (0409-3299-45) · 0409-3299-25
  • 25 VIAL in 1 TRAY (0409-3299-26) / 50 mL in 1 VIAL (0409-3299-46) · 0409-3299-26

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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