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
- 51754-2004_2b86b9e8-48ba-4a72-b705-48c2751016e6
- Product NDC
- 51754-2004
- Form
- INJECTION
- Composition / generic term
- Potassium Acetate
- Labeler
- Exela Pharma Sciences, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230801
- Source listing expiry
- 20261231
Source-listed ingredients
- POTASSIUM ACETATE — 200 meq/100mL
These values do not establish equivalence or a dose recommendation.
Packages
- 25 VIAL, GLASS in 1 CARTON (51754-2004-4) / 100 mL in 1 VIAL, GLASS · 51754-2004-4
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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