plasma-lyte 148 (ph 7.4)

Generic: sodium chloride, sodium gluconate, sodium acetate, potassium chloride, magnesium chloride

Labeler: baxter healthcare corporation
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE Inactive Finished

Drug Facts

Product Profile

Brand Name plasma-lyte 148 (ph 7.4)
Generic Name sodium chloride, sodium gluconate, sodium acetate, potassium chloride, magnesium chloride
Labeler baxter healthcare corporation
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

magnesium chloride 30 mg/100mL, potassium chloride 37 mg/100mL, sodium acetate 368 mg/100mL, sodium chloride 526 mg/100mL, sodium gluconate 502 mg/100mL

Manufacturer
Baxter Healthcare Corporation

Identifiers & Regulatory

Product NDC 0338-9593
Product ID 0338-9593_0fe5a11d-9640-4645-8d45-488a04ea6550
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE
Listing Expiration 2026-12-31
Marketing Start 2024-11-08

Pharmacologic Class

Classes
calculi dissolution agent [epc] increased large intestinal motility [pe] inhibition large intestine fluid/electrolyte absorption [pe] inhibition small intestine fluid/electrolyte absorption [pe] magnesium ion exchange activity [moa] osmotic activity [moa] osmotic laxative [epc] potassium compounds [cs] potassium salt [epc] stimulation large intestine fluid/electrolyte secretion [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03389593
Hyphenated Format 0338-9593

Supplemental Identifiers

RxCUI
801109 801357
UNII
02F3473H9O 660YQ98I10 4550K0SC9B 451W47IQ8X R6Q3791S76

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 plasma-lyte 148 (ph 7.4) (source: ndc)
Generic Name sodium chloride, sodium gluconate, sodium acetate, potassium chloride, magnesium chloride (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 30 mg/100mL
  • 37 mg/100mL
  • 368 mg/100mL
  • 526 mg/100mL
  • 502 mg/100mL
source: ndc
Packaging
  • 10 BAG in 1 CARTON (0338-9593-10) / 1000 mL in 1 BAG (0338-9593-01)
source: ndc

Packages (1)

0338-9593-10 10 BAG in 1 CARTON (0338-9593-10) / 1000 mL in 1 BAG (0338-9593-01)

Ingredients (5)

magnesium chloride (30 mg/100mL) potassium chloride (37 mg/100mL) sodium acetate (368 mg/100mL) sodium chloride (526 mg/100mL) sodium gluconate (502 mg/100mL)

Linked Drug Pages (1)

Plasma-Lyte 148 (pH 7.4) ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "0fe5a11d-9640-4645-8d45-488a04ea6550", "openfda": {"unii": ["02F3473H9O", "660YQ98I10", "4550K0SC9B", "451W47IQ8X", "R6Q3791S76"], "rxcui": ["801109", "801357"], "spl_set_id": ["fe935c8d-f42d-42e4-8665-0dc66829f231"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BAG in 1 CARTON (0338-9593-10)  / 1000 mL in 1 BAG (0338-9593-01)", "package_ndc": "0338-9593-10", "marketing_start_date": "20241108"}], "brand_name": "Plasma-Lyte 148 (pH 7.4)", "product_id": "0338-9593_0fe5a11d-9640-4645-8d45-488a04ea6550", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Calculi Dissolution Agent [EPC]", "Increased Large Intestinal Motility [PE]", "Increased Large Intestinal Motility [PE]", "Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]", "Magnesium Ion Exchange Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Osmotic Laxative [EPC]", "Osmotic Laxative [EPC]", "Potassium Compounds [CS]", "Potassium Salt [EPC]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "product_ndc": "0338-9593", "generic_name": "Sodium Chloride, Sodium Gluconate, Sodium Acetate, Potassium Chloride, Magnesium Chloride", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Plasma-Lyte 148 (pH 7.4)", "active_ingredients": [{"name": "MAGNESIUM CHLORIDE", "strength": "30 mg/100mL"}, {"name": "POTASSIUM CHLORIDE", "strength": "37 mg/100mL"}, {"name": "SODIUM ACETATE", "strength": "368 mg/100mL"}, {"name": "SODIUM CHLORIDE", "strength": "526 mg/100mL"}, {"name": "SODIUM GLUCONATE", "strength": "502 mg/100mL"}], "marketing_category": "UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE", "marketing_start_date": "20241108", "listing_expiration_date": "20261231"}