dextrose and electrolyte no. 48

Generic: sodium lactate, potassium chloride, magnesium chloride, monobasic potassium phosphate, sodium chloride and dextrose monohydrate

Labeler: baxter healthcare company
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name dextrose and electrolyte no. 48
Generic Name sodium lactate, potassium chloride, magnesium chloride, monobasic potassium phosphate, sodium chloride and dextrose monohydrate
Labeler baxter healthcare company
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

dextrose monohydrate 5 g/100mL, magnesium chloride 31 mg/100mL, potassium chloride 141 mg/100mL, potassium phosphate, monobasic 20 mg/100mL, sodium chloride 12 mg/100mL, sodium lactate 260 mg/100mL

Manufacturer
Baxter Healthcare Company

Identifiers & Regulatory

Product NDC 0338-0143
Product ID 0338-0143_83a474ed-d005-435f-8ff9-415d4a53ffd6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA017484
Listing Expiration 2026-12-31
Marketing Start 1979-02-02

Pharmacologic Class

Classes
acidifying activity [moa] increased large intestinal motility [pe] inhibition large intestine fluid/electrolyte absorption [pe] osmotic activity [moa] osmotic laxative [epc] potassium compounds [cs] potassium salt [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03380143
Hyphenated Format 0338-0143

Supplemental Identifiers

RxCUI
807396
UNII
LX22YL083G 02F3473H9O 660YQ98I10 4J9FJ0HL51 451W47IQ8X TU7HW0W0QT

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name dextrose and electrolyte no. 48 (source: ndc)
Generic Name sodium lactate, potassium chloride, magnesium chloride, monobasic potassium phosphate, sodium chloride and dextrose monohydrate (source: ndc)
Application Number NDA017484 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 5 g/100mL
  • 31 mg/100mL
  • 141 mg/100mL
  • 20 mg/100mL
  • 12 mg/100mL
  • 260 mg/100mL
source: ndc
Packaging
  • 500 mL in 1 BAG (0338-0143-03)
source: ndc

Packages (1)

Ingredients (6)

dextrose monohydrate (5 g/100mL) magnesium chloride (31 mg/100mL) potassium chloride (141 mg/100mL) potassium phosphate, monobasic (20 mg/100mL) sodium chloride (12 mg/100mL) sodium lactate (260 mg/100mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "83a474ed-d005-435f-8ff9-415d4a53ffd6", "openfda": {"unii": ["LX22YL083G", "02F3473H9O", "660YQ98I10", "4J9FJ0HL51", "451W47IQ8X", "TU7HW0W0QT"], "rxcui": ["807396"], "spl_set_id": ["b283a454-0c20-4fbf-92d3-dae1f3cd3cad"], "manufacturer_name": ["Baxter Healthcare Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 mL in 1 BAG (0338-0143-03)", "package_ndc": "0338-0143-03", "marketing_start_date": "19790202"}], "brand_name": "Dextrose and Electrolyte No. 48", "product_id": "0338-0143_83a474ed-d005-435f-8ff9-415d4a53ffd6", "dosage_form": "INJECTION", "pharm_class": ["Acidifying Activity [MoA]", "Increased Large Intestinal Motility [PE]", "Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Osmotic Laxative [EPC]", "Potassium Compounds [CS]", "Potassium Salt [EPC]"], "product_ndc": "0338-0143", "generic_name": "Sodium Lactate, Potassium Chloride, Magnesium Chloride, Monobasic Potassium Phosphate, Sodium Chloride and Dextrose monohydrate", "labeler_name": "Baxter Healthcare Company", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dextrose and Electrolyte No. 48", "active_ingredients": [{"name": "DEXTROSE MONOHYDRATE", "strength": "5 g/100mL"}, {"name": "MAGNESIUM CHLORIDE", "strength": "31 mg/100mL"}, {"name": "POTASSIUM CHLORIDE", "strength": "141 mg/100mL"}, {"name": "POTASSIUM PHOSPHATE, MONOBASIC", "strength": "20 mg/100mL"}, {"name": "SODIUM CHLORIDE", "strength": "12 mg/100mL"}, {"name": "SODIUM LACTATE", "strength": "260 mg/100mL"}], "application_number": "NDA017484", "marketing_category": "NDA", "marketing_start_date": "19790202", "listing_expiration_date": "20261231"}