sodium chloride

Generic: sodium chloride

Labeler: hospira, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name sodium chloride
Generic Name sodium chloride
Labeler hospira, inc.
Dosage Form INJECTION, SOLUTION, CONCENTRATE
Routes
INTRAVENOUS
Active Ingredients

sodium chloride 234 mg/mL

Manufacturer
Hospira, Inc.

Identifiers & Regulatory

Product NDC 0409-1141
Product ID 0409-1141_4b8e6f49-4268-4654-9b7d-8dcd235aa040
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA018897
Listing Expiration 2026-12-31
Marketing Start 2005-04-30

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 04091141
Hyphenated Format 0409-1141

Supplemental Identifiers

RxCUI
313016
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 NDA018897 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 234 mg/mL
source: ndc
Packaging
  • 25 VIAL, PHARMACY BULK PACKAGE in 1 CASE (0409-1141-02) / 100 mL in 1 VIAL, PHARMACY BULK PACKAGE (0409-1141-12)
source: ndc

Packages (1)

0409-1141-02 25 VIAL, PHARMACY BULK PACKAGE in 1 CASE (0409-1141-02) / 100 mL in 1 VIAL, PHARMACY BULK PACKAGE (0409-1141-12)

Ingredients (1)

sodium chloride (234 mg/mL)

Linked Drug Pages (1)

SODIUM CHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "4b8e6f49-4268-4654-9b7d-8dcd235aa040", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["313016"], "spl_set_id": ["af6aebad-ef03-4d19-9a40-18e5a278b812"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, PHARMACY BULK PACKAGE in 1 CASE (0409-1141-02)  / 100 mL in 1 VIAL, PHARMACY BULK PACKAGE (0409-1141-12)", "package_ndc": "0409-1141-02", "marketing_start_date": "20050430"}], "brand_name": "SODIUM CHLORIDE", "product_id": "0409-1141_4b8e6f49-4268-4654-9b7d-8dcd235aa040", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "0409-1141", "generic_name": "SODIUM CHLORIDE", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SODIUM CHLORIDE", "active_ingredients": [{"name": "SODIUM CHLORIDE", "strength": "234 mg/mL"}], "application_number": "NDA018897", "marketing_category": "NDA", "marketing_start_date": "20050430", "listing_expiration_date": "20261231"}