United States · FDA National Drug Code directory
Ionosol MB and Dextrose
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
- 0990-7372_f6e10cf9-7244-440c-88a3-a100a51bb74c
- Product NDC
- 0990-7372
- Form
- INJECTION, SOLUTION
- Composition / generic term
- DEXTROSE MONOHYDRATE, SODIUM LACTATE, POTASSIUM CHLORIDE, MAGNESIUM CHLORIDE, POTASSIUM PHOSPHATE, MONOBASIC, and SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE
- Labeler
- ICU Medical Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20190701
- Source listing expiry
- 20271231
Source-listed ingredients
- DEXTROSE MONOHYDRATE — 5 g/100mL
- SODIUM LACTATE — 260 mg/100mL
- POTASSIUM CHLORIDE — 141 mg/100mL
- MAGNESIUM CHLORIDE — 30 mg/100mL
- MONOBASIC POTASSIUM PHOSPHATE — 15 mg/100mL
- SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE — 25 mg/100mL
These values do not establish equivalence or a dose recommendation.
Packages
- 24 POUCH in 1 CASE (0990-7372-03) / 1 BAG in 1 POUCH / 500 mL in 1 BAG · 0990-7372-03
- 24 POUCH in 1 CASE (0990-7372-62) / 1 BAG in 1 POUCH / 250 mL in 1 BAG · 0990-7372-62
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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