sodium chloride

Generic: sodium chloride

Labeler: fresenius kabi usa, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sodium chloride
Generic Name sodium chloride
Labeler fresenius kabi usa, llc
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

sodium chloride 1125 mg/250mL

Manufacturer
Fresenius Kabi USA, LLC

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
increased large intestinal motility [pe] inhibition large intestine fluid/electrolyte absorption [pe] osmotic activity [moa] osmotic laxative [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 65219230
Hyphenated Format 65219-230

Supplemental Identifiers

RxCUI
1807548 1807549 1807550 1807551
UNII
451W47IQ8X

Packaging Origin

Original Packager
true

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
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 1125 mg/250mL
source: ndc
Packaging
  • 30 BAG in 1 CASE (65219-230-25) / 250 mL in 1 BAG (65219-230-01)
source: ndc

Packages (1)

Ingredients (1)

sodium chloride (1125 mg/250mL)

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"}