Elliotts B
Active substance: SODIUM CHLORIDE, SODIUM BICARBONATE, ANHYDROUS DEXTROSE, MAGNESIUM SULFATE, UNSPECIFIED FORM, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, SODIUM PHOSPHATE
INJECTION · SODIUM CHLORIDE 73 mg/10mL, SODIUM BICARBONATE 19 mg/10mL, ANHYDROUS DEXTROSE 8 mg/10mL, MAGNESIUM SULFATE, UNSPECIFIED FORM 3 mg/10mL, POTASSIUM CHLORIDE 3 mg/10mL, CALCIUM CHLORIDE 2 mg/10mL, SODIUM PHOSPHATE 2 mg/10mL
United StatesActive
Marketing holder: Lukare Medical, LLC
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
- Countries with the substance registered: 1
Composition
- SODIUM CHLORIDE · 73 mg/10mL
- SODIUM BICARBONATE · 19 mg/10mL
- ANHYDROUS DEXTROSE · 8 mg/10mL
- MAGNESIUM SULFATE, UNSPECIFIED FORM · 3 mg/10mL
- POTASSIUM CHLORIDE · 3 mg/10mL
- CALCIUM CHLORIDE · 2 mg/10mL
- SODIUM PHOSPHATE · 2 mg/10mL
Registration
- Registration number
- 55792-007
- Registration status
- Active
- Dispensing
- Prescription only
- Route
- INTRATHECAL
Sources
- product · openFDA NDC · 55792-007 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 55792-007 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 55792-007 · Verified 2026-10-09 · open in source
- ingredients.1 · openFDA NDC · 55792-007 · Verified 2026-10-09 · open in source
- ingredients.2 · openFDA NDC · 55792-007 · Verified 2026-10-09 · open in source
- ingredients.3 · openFDA NDC · 55792-007 · Verified 2026-10-09 · open in source
- ingredients.4 · openFDA NDC · 55792-007 · Verified 2026-10-09 · open in source
- ingredients.5 · openFDA NDC · 55792-007 · Verified 2026-10-09 · open in source
- ingredients.6 · openFDA NDC · 55792-007 · Verified 2026-10-09 · open in source