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 1125 mg/250mL
Manufacturer
Identifiers & Regulatory
Product NDC
65219-230
Product ID
65219-230_02cd6592-b609-44d9-9fb3-3fb077e9a4fb
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208122
Listing Expiration
2026-12-31
Marketing Start
2018-07-23
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
65219230
Hyphenated Format
65219-230
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
ANDA208122 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1125 mg/250mL
Packaging
- 30 BAG in 1 CASE (65219-230-25) / 250 mL in 1 BAG (65219-230-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "02cd6592-b609-44d9-9fb3-3fb077e9a4fb", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["1807548", "1807549", "1807550", "1807551"], "spl_set_id": ["239a5af1-7498-480f-862c-ab7c3d89d183"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 BAG in 1 CASE (65219-230-25) / 250 mL in 1 BAG (65219-230-01)", "package_ndc": "65219-230-25", "marketing_start_date": "20211130"}], "brand_name": "Sodium chloride", "product_id": "65219-230_02cd6592-b609-44d9-9fb3-3fb077e9a4fb", "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": "65219-230", "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": "1125 mg/250mL"}], "application_number": "ANDA208122", "marketing_category": "ANDA", "marketing_start_date": "20180723", "listing_expiration_date": "20261231"}