sodium chloride
Generic: sodium chloride
Labeler: fresenius kabi usa, llcDrug Facts
Product Profile
Brand Name
sodium chloride
Generic Name
sodium chloride
Labeler
fresenius kabi usa, llc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
sodium chloride .9 g/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
65219-506
Product ID
65219-506_53843388-e3bc-4344-87aa-b345680ec27b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA213688
Listing Expiration
2026-12-31
Marketing Start
2025-03-03
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
65219506
Hyphenated Format
65219-506
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
ANDA213688 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .9 g/100mL
Packaging
- 4 BAG in 1 CASE (65219-506-30) / 3000 mL in 1 BAG (65219-506-03)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["IRRIGATION"], "spl_id": "53843388-e3bc-4344-87aa-b345680ec27b", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["486515"], "spl_set_id": ["ce0c8c6f-734a-400f-9b60-a3b1e263f25f"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 BAG in 1 CASE (65219-506-30) / 3000 mL in 1 BAG (65219-506-03)", "package_ndc": "65219-506-30", "marketing_start_date": "20250303"}], "brand_name": "Sodium chloride", "product_id": "65219-506_53843388-e3bc-4344-87aa-b345680ec27b", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "65219-506", "generic_name": "SODIUM CHLORIDE", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium chloride", "active_ingredients": [{"name": "SODIUM CHLORIDE", "strength": ".9 g/100mL"}], "application_number": "ANDA213688", "marketing_category": "ANDA", "marketing_start_date": "20250303", "listing_expiration_date": "20261231"}