sodium chloride
Generic: sodium chloride
Labeler: icu medical inc.Drug Facts
Product Profile
Brand Name
sodium chloride
Generic Name
sodium chloride
Labeler
icu medical inc.
Dosage Form
IRRIGANT
Routes
Active Ingredients
sodium chloride 900 mg/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
0990-6138
Product ID
0990-6138_6c376c61-a98d-4220-b82f-b1e610f3479a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA017514
Marketing Start
2019-08-01
Marketing End
2026-05-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
09906138
Hyphenated Format
0990-6138
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
sodium chloride (source: ndc)
Generic Name
sodium chloride (source: ndc)
Application Number
NDA017514 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 900 mg/100mL
Packaging
- 24 BOTTLE, PLASTIC in 1 CASE (0990-6138-03) / 500 mL in 1 BOTTLE, PLASTIC
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["IRRIGATION"], "spl_id": "6c376c61-a98d-4220-b82f-b1e610f3479a", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["486515"], "spl_set_id": ["3cfdeee0-ff14-4341-8396-b11c2a037c60"], "manufacturer_name": ["ICU Medical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 BOTTLE, PLASTIC in 1 CASE (0990-6138-03) / 500 mL in 1 BOTTLE, PLASTIC", "package_ndc": "0990-6138-03", "marketing_end_date": "20260501", "marketing_start_date": "20191001"}], "brand_name": "Sodium Chloride", "product_id": "0990-6138_6c376c61-a98d-4220-b82f-b1e610f3479a", "dosage_form": "IRRIGANT", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "0990-6138", "generic_name": "SODIUM CHLORIDE", "labeler_name": "ICU Medical Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Chloride", "active_ingredients": [{"name": "SODIUM CHLORIDE", "strength": "900 mg/100mL"}], "application_number": "NDA017514", "marketing_category": "NDA", "marketing_end_date": "20260501", "marketing_start_date": "20190801"}