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
65219-218
Product ID
65219-218_d5c0c612-d7b8-458f-8ad3-d3999b3bd89d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA207310
Listing Expiration
2027-12-31
Marketing Start
2017-09-19
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
65219218
Hyphenated Format
65219-218
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
- 60 BAG in 1 CASE (65219-218-50) / 50 mL in 1 BAG (65219-218-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "d5c0c612-d7b8-458f-8ad3-d3999b3bd89d", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["1807631", "1807632", "1807633", "1807634"], "spl_set_id": ["d98bf9f7-30ec-4927-a577-cabad192cb18"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 BAG in 1 CASE (65219-218-50) / 50 mL in 1 BAG (65219-218-01)", "package_ndc": "65219-218-50", "marketing_start_date": "20211117"}], "brand_name": "Sodium chloride", "product_id": "65219-218_d5c0c612-d7b8-458f-8ad3-d3999b3bd89d", "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": "65219-218", "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": "20271231"}