plasma-lyte a

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

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

Drug Facts

Product Profile

Brand Name plasma-lyte a
Generic Name sodium chloride, sodium gluconate, sodium acetate, potassium chloride and 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 0338-0221
Product ID 0338-0221_888f2003-1dc2-4bc0-9b3b-ebe3948b9328
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA017378
Listing Expiration 2026-12-31
Marketing Start 1979-02-02

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 03380221
Hyphenated Format 0338-0221

Supplemental Identifiers

RxCUI
801109 801112
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 a (source: ndc)
Generic Name sodium chloride, sodium gluconate, sodium acetate, potassium chloride and magnesium chloride (source: ndc)
Application Number NDA017378 (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
  • 500 mL in 1 BAG (0338-0221-03)
  • 1000 mL in 1 BAG (0338-0221-04)
source: ndc

Packages (2)

0338-0221-03 500 mL in 1 BAG (0338-0221-03) 0338-0221-04 1000 mL in 1 BAG (0338-0221-04)

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 A ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "888f2003-1dc2-4bc0-9b3b-ebe3948b9328", "openfda": {"unii": ["02F3473H9O", "660YQ98I10", "4550K0SC9B", "451W47IQ8X", "R6Q3791S76"], "rxcui": ["801109", "801112"], "spl_set_id": ["6ec9e61c-2c26-402f-8604-f446b2e34058"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 mL in 1 BAG (0338-0221-03)", "package_ndc": "0338-0221-03", "marketing_start_date": "19790202"}, {"sample": false, "description": "1000 mL in 1 BAG (0338-0221-04)", "package_ndc": "0338-0221-04", "marketing_start_date": "19790202"}], "brand_name": "Plasma-Lyte A", "product_id": "0338-0221_888f2003-1dc2-4bc0-9b3b-ebe3948b9328", "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": "0338-0221", "generic_name": "Sodium Chloride, Sodium Gluconate, Sodium Acetate, Potassium Chloride and Magnesium Chloride", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Plasma-Lyte A", "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"}], "application_number": "NDA017378", "marketing_category": "NDA", "marketing_start_date": "19790202", "listing_expiration_date": "20261231"}