lactated ringers and dextrose
Generic: sodium chloride, sodium lactate, potassium chloride, calcium chloride, and dextrose monohydrate
Labeler: hf acquisition co llc, dba healthfirstDrug Facts
Product Profile
Brand Name
lactated ringers and dextrose
Generic Name
sodium chloride, sodium lactate, potassium chloride, calcium chloride, and dextrose monohydrate
Labeler
hf acquisition co llc, dba healthfirst
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
51662-1521
Product ID
51662-1521_a62cf623-9b8b-37e0-e053-2995a90add5b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA017608
Listing Expiration
2026-12-31
Marketing Start
2020-05-21
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
516621521
Hyphenated Format
51662-1521
Supplemental Identifiers
RxCUI
UNII
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
NDA017608 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/100mL
- 5 g/100mL
- 30 mg/100mL
- 600 mg/100mL
- 310 mg/100mL
Packaging
- 1000 mL in 1 BAG (51662-1521-1)
Packages (1)
Ingredients (5)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "a62cf623-9b8b-37e0-e053-2995a90add5b", "openfda": {"unii": ["M4I0D6VV5M", "LX22YL083G", "660YQ98I10", "451W47IQ8X", "TU7HW0W0QT"], "rxcui": ["847627"], "spl_set_id": ["a62cf623-9b8a-37e0-e053-2995a90add5b"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 mL in 1 BAG (51662-1521-1)", "package_ndc": "51662-1521-1", "marketing_start_date": "20200521"}], "brand_name": "LACTATED RINGERS AND DEXTROSE", "product_id": "51662-1521_a62cf623-9b8b-37e0-e053-2995a90add5b", "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]", "Potassium Compounds [CS]", "Potassium Salt [EPC]"], "product_ndc": "51662-1521", "generic_name": "SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, AND DEXTROSE MONOHYDRATE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "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": "NDA017608", "marketing_category": "NDA", "marketing_start_date": "20200521", "listing_expiration_date": "20261231"}