dextrose and electrolyte no. 48
Generic: sodium lactate, potassium chloride, magnesium chloride, monobasic potassium phosphate, sodium chloride and dextrose monohydrate
Labeler: baxter healthcare companyDrug 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
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
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
03380143
Hyphenated Format
0338-0143
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 5 g/100mL
- 31 mg/100mL
- 141 mg/100mL
- 20 mg/100mL
- 12 mg/100mL
- 260 mg/100mL
Packaging
- 500 mL in 1 BAG (0338-0143-03)
Packages (1)
Ingredients (6)
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"}