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 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
65219-328
Product ID
65219-328_904e72e0-2558-4548-8ddd-8c6877c23b98
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA207310
Listing Expiration
2026-12-31
Marketing Start
2017-09-19
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
65219328
Hyphenated Format
65219-328
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
ANDA207310 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 9 mg/mL
Packaging
- 10 BAG in 1 CASE (65219-328-50) / 1000 mL in 1 BAG (65219-328-10)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "904e72e0-2558-4548-8ddd-8c6877c23b98", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["1807634", "1807639"], "spl_set_id": ["2e5fe9f4-78e5-4af4-8bf9-9680e5dc5e88"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BAG in 1 CASE (65219-328-50) / 1000 mL in 1 BAG (65219-328-10)", "package_ndc": "65219-328-50", "marketing_start_date": "20230911"}], "brand_name": "Sodium Chloride", "product_id": "65219-328_904e72e0-2558-4548-8ddd-8c6877c23b98", "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": "65219-328", "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 mg/mL"}], "application_number": "ANDA207310", "marketing_category": "ANDA", "marketing_start_date": "20170919", "listing_expiration_date": "20261231"}