United States · FDA National Drug Code directory
Sodium Phosphates
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
- 0517-7350_4b71a79f-83da-45b0-a398-4833ecc17ba4
- Product NDC
- 0517-7350
- Form
- INJECTION, SOLUTION
- Composition / generic term
- sodium phosphate, monobasic, monohydrate and sodium phosphate, dibasic anhydrous
- Labeler
- American Regent, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240621
- Source listing expiry
- 20261231
Source-listed ingredients
- SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE — 276 mg/mL
- SODIUM PHOSPHATE, DIBASIC, ANHYDROUS — 142 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-7350-25) / 50 mL in 1 VIAL, SINGLE-DOSE (0517-7350-01) · 0517-7350-25
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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