lactated ringers and dextrose
Generic: sodium chloride, sodium lactate, potassium chloride, calcium chloride, and dextrose monohydrate
Labeler: fresenius kabi usa, llcDrug Facts
Product Profile
Brand Name
lactated ringers and dextrose
Generic Name
sodium chloride, sodium lactate, potassium chloride, calcium chloride, and dextrose monohydrate
Labeler
fresenius kabi usa, llc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
calcium chloride 20 mg/100mL, dextrose monohydrate 5 g/100mL, potassium chloride 30 mg/100mL, sodium chloride 600 mg/100mL, sodium lactate 310 mg/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
65219-241
Product ID
65219-241_b13e4afe-9bf1-4bf8-9674-e53ae5cb0fce
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210332
Listing Expiration
2026-12-31
Marketing Start
2022-03-28
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
65219241
Hyphenated Format
65219-241
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
lactated ringers and dextrose (source: ndc)
Generic Name
sodium chloride, sodium lactate, potassium chloride, calcium chloride, and dextrose monohydrate (source: ndc)
Application Number
ANDA210332 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/100mL
- 5 g/100mL
- 30 mg/100mL
- 600 mg/100mL
- 310 mg/100mL
Packaging
- 10 BAG in 1 CASE (65219-241-10) / 1000 mL in 1 BAG (65219-241-00)
Packages (1)
Ingredients (5)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "b13e4afe-9bf1-4bf8-9674-e53ae5cb0fce", "openfda": {"unii": ["M4I0D6VV5M", "TU7HW0W0QT", "660YQ98I10", "451W47IQ8X", "LX22YL083G"], "rxcui": ["847627"], "spl_set_id": ["1b912c7e-f005-4af4-b683-083440964249"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BAG in 1 CASE (65219-241-10) / 1000 mL in 1 BAG (65219-241-00)", "package_ndc": "65219-241-10", "marketing_start_date": "20220328"}], "brand_name": "Lactated Ringers and Dextrose", "product_id": "65219-241_b13e4afe-9bf1-4bf8-9674-e53ae5cb0fce", "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": "65219-241", "generic_name": "SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, and DEXTROSE MONOHYDRATE", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lactated Ringers and Dextrose", "active_ingredients": [{"name": "CALCIUM CHLORIDE", "strength": "20 mg/100mL"}, {"name": "DEXTROSE MONOHYDRATE", "strength": "5 g/100mL"}, {"name": "POTASSIUM CHLORIDE", "strength": "30 mg/100mL"}, {"name": "SODIUM CHLORIDE", "strength": "600 mg/100mL"}, {"name": "SODIUM LACTATE", "strength": "310 mg/100mL"}], "application_number": "ANDA210332", "marketing_category": "ANDA", "marketing_start_date": "20220328", "listing_expiration_date": "20261231"}