potassium chloride in lactated ringers and dextrose

Generic: potassium chloride, sodium chloride, calcium chloride, sodium lactate, and dextrose monohydrate

Labeler: icu medical inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name potassium chloride in lactated ringers and dextrose
Generic Name potassium chloride, sodium chloride, calcium chloride, sodium lactate, and dextrose monohydrate
Labeler icu medical inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

calcium chloride .2 g/1000mL, dextrose monohydrate 50 g/1000mL, potassium chloride 1.79 g/1000mL, sodium chloride 6 g/1000mL, sodium lactate 3.1 g/1000mL

Manufacturer
ICU Medical Inc.

Identifiers & Regulatory

Product NDC 0990-7111
Product ID 0990-7111_fb53b802-9589-46e1-b404-b51c4ac61f5b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA019685
Listing Expiration 2026-12-31
Marketing Start 2019-11-25

Pharmacologic Class

Classes
blood coagulation factor [epc] calcium [cs] cations divalent [cs] increased coagulation factor activity [pe] increased large intestinal motility [pe] inhibition large intestine fluid/electrolyte absorption [pe] osmotic activity [moa] osmotic laxative [epc] phosphate binder [epc] phosphate chelating activity [moa] potassium compounds [cs] potassium salt [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09907111
Hyphenated Format 0990-7111

Supplemental Identifiers

RxCUI
847626
UNII
M4I0D6VV5M LX22YL083G 660YQ98I10 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 potassium chloride in lactated ringers and dextrose (source: ndc)
Generic Name potassium chloride, sodium chloride, calcium chloride, sodium lactate, and dextrose monohydrate (source: ndc)
Application Number NDA019685 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • .2 g/1000mL
  • 50 g/1000mL
  • 1.79 g/1000mL
  • 6 g/1000mL
  • 3.1 g/1000mL
source: ndc
Packaging
  • 12 POUCH in 1 CASE (0990-7111-09) / 1 BAG in 1 POUCH / 1000 mL in 1 BAG
source: ndc

Packages (1)

Ingredients (5)

calcium chloride (.2 g/1000mL) dextrose monohydrate (50 g/1000mL) potassium chloride (1.79 g/1000mL) sodium chloride (6 g/1000mL) sodium lactate (3.1 g/1000mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "fb53b802-9589-46e1-b404-b51c4ac61f5b", "openfda": {"unii": ["M4I0D6VV5M", "LX22YL083G", "660YQ98I10", "451W47IQ8X", "TU7HW0W0QT"], "rxcui": ["847626"], "spl_set_id": ["237b39fa-916e-4a54-99c8-4ae9ad54f056"], "manufacturer_name": ["ICU Medical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 POUCH in 1 CASE (0990-7111-09)  / 1 BAG in 1 POUCH / 1000 mL in 1 BAG", "package_ndc": "0990-7111-09", "marketing_start_date": "20191125"}], "brand_name": "Potassium Chloride in Lactated Ringers and Dextrose", "product_id": "0990-7111_fb53b802-9589-46e1-b404-b51c4ac61f5b", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Blood Coagulation Factor [EPC]", "Calcium [CS]", "Cations", "Divalent [CS]", "Increased Coagulation Factor Activity [PE]", "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]", "Osmotic Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Osmotic Laxative [EPC]", "Osmotic Laxative [EPC]", "Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]", "Potassium Compounds [CS]", "Potassium Salt [EPC]"], "product_ndc": "0990-7111", "generic_name": "POTASSIUM CHLORIDE, SODIUM CHLORIDE, CALCIUM CHLORIDE, SODIUM LACTATE, and DEXTROSE MONOHYDRATE", "labeler_name": "ICU Medical Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride in Lactated Ringers and Dextrose", "active_ingredients": [{"name": "CALCIUM CHLORIDE", "strength": ".2 g/1000mL"}, {"name": "DEXTROSE MONOHYDRATE", "strength": "50 g/1000mL"}, {"name": "POTASSIUM CHLORIDE", "strength": "1.79 g/1000mL"}, {"name": "SODIUM CHLORIDE", "strength": "6 g/1000mL"}, {"name": "SODIUM LACTATE", "strength": "3.1 g/1000mL"}], "application_number": "NDA019685", "marketing_category": "NDA", "marketing_start_date": "20191125", "listing_expiration_date": "20261231"}