United States · FDA National Drug Code directory

Potassium 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
0409-8183_b778ca66-055a-495c-a922-7abcd5435901
Product NDC
0409-8183
Form
INJECTION, SOLUTION, CONCENTRATE
Composition / generic term
POTASSIUM ACETATE
Labeler
Hospira, Inc.
Marketing category
NDA
Marketing start / end (source format)
20140327
Source listing expiry
20271231

Source-listed ingredients

  • POTASSIUM ACETATE — 3.93 g/20mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-8183-25) / 20 mL in 1 VIAL, SINGLE-DOSE (0409-8183-15) · 0409-8183-25

Source and coverage

Open FDA National Drug Code directory

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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Potassium Acetate — United States | Molindra Medicines