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
- 65219-510_67c83f58-73cd-47d2-8dbc-e0fd8331c6e7
- Product NDC
- 65219-510
- Form
- INJECTION, SOLUTION, CONCENTRATE
- Composition / generic term
- POTASSIUM ACETATE
- Labeler
- Fresenius Kabi USA, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20241127
- Source listing expiry
- 20261231
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 (65219-510-20) / 20 mL in 1 VIAL, SINGLE-DOSE (65219-510-02) · 65219-510-20
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.
Browse United States records →