lactated ringers
Generic: sodium chloride, sodium lactate, potassium chloride, and calcium chloride
Labeler: asclemed usa, inc.Drug Facts
Product Profile
Brand Name
lactated ringers
Generic Name
sodium chloride, sodium lactate, potassium chloride, and calcium chloride
Labeler
asclemed usa, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
calcium chloride 20 mg/100mL, potassium chloride 30 mg/100mL, sodium chloride 600 mg/100mL, sodium lactate 310 mg/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
76420-129
Product ID
76420-129_b2c9498d-2899-3ee5-e053-2a95a90af167
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA017641
Listing Expiration
2026-12-31
Marketing Start
2019-06-24
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
76420129
Hyphenated Format
76420-129
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 (source: ndc)
Generic Name
sodium chloride, sodium lactate, potassium chloride, and calcium chloride (source: ndc)
Application Number
NDA017641 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/100mL
- 30 mg/100mL
- 600 mg/100mL
- 310 mg/100mL
Packaging
- 1000 mL in 1 BAG (76420-129-01)
Packages (1)
Ingredients (4)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "b2c9498d-2899-3ee5-e053-2a95a90af167", "openfda": {"unii": ["M4I0D6VV5M", "660YQ98I10", "451W47IQ8X", "TU7HW0W0QT"], "rxcui": ["847630"], "spl_set_id": ["afac6cc5-1ced-4639-b6f6-86f40ef5c30e"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1000 mL in 1 BAG (76420-129-01)", "package_ndc": "76420-129-01", "marketing_start_date": "20201029"}], "brand_name": "Lactated Ringers", "product_id": "76420-129_b2c9498d-2899-3ee5-e053-2a95a90af167", "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": "76420-129", "generic_name": "SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, and CALCIUM CHLORIDE", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lactated Ringers", "active_ingredients": [{"name": "CALCIUM CHLORIDE", "strength": "20 mg/100mL"}, {"name": "POTASSIUM CHLORIDE", "strength": "30 mg/100mL"}, {"name": "SODIUM CHLORIDE", "strength": "600 mg/100mL"}, {"name": "SODIUM LACTATE", "strength": "310 mg/100mL"}], "application_number": "NDA017641", "marketing_category": "NDA", "marketing_start_date": "20190624", "listing_expiration_date": "20261231"}