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
Routes
INTRAVENOUS
Active Ingredients

sodium chloride 900 mg/100mL

Manufacturer
Hospira, Inc.

Identifiers & Regulatory

Product NDC 0409-7101
Product ID 0409-7101_f233e72c-072d-4a43-857a-f4d5791e1a73
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA019465
Listing Expiration 2027-12-31
Marketing Start 2005-06-30

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 04097101
Hyphenated Format 0409-7101

Supplemental Identifiers

RxCUI
1807547 1807631 1807632 1807633
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 NDA019465 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 900 mg/100mL
source: ndc
Packaging
  • 24 POUCH in 1 CASE (0409-7101-02) / 1 BAG in 1 POUCH / 250 mL in 1 BAG (0409-7101-04)
  • 10 POUCH in 1 CASE (0409-7101-66) / 5 BAG in 1 POUCH / 50 mL in 1 BAG (0409-7101-68)
  • 10 POUCH in 1 CASE (0409-7101-67) / 5 BAG in 1 POUCH / 100 mL in 1 BAG (0409-7101-69)
source: ndc

Packages (3)

0409-7101-02 24 POUCH in 1 CASE (0409-7101-02) / 1 BAG in 1 POUCH / 250 mL in 1 BAG (0409-7101-04) 0409-7101-66 10 POUCH in 1 CASE (0409-7101-66) / 5 BAG in 1 POUCH / 50 mL in 1 BAG (0409-7101-68) 0409-7101-67 10 POUCH in 1 CASE (0409-7101-67) / 5 BAG in 1 POUCH / 100 mL in 1 BAG (0409-7101-69)

Ingredients (1)

sodium chloride (900 mg/100mL)

Linked Drug Pages (1)

Sodium Chloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "f233e72c-072d-4a43-857a-f4d5791e1a73", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["1807547", "1807631", "1807632", "1807633"], "spl_set_id": ["a2a964f7-c3ec-4dfb-e3a0-6d8136a80397"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 POUCH in 1 CASE (0409-7101-02)  / 1 BAG in 1 POUCH / 250 mL in 1 BAG (0409-7101-04)", "package_ndc": "0409-7101-02", "marketing_start_date": "20050630"}, {"sample": false, "description": "10 POUCH in 1 CASE (0409-7101-66)  / 5 BAG in 1 POUCH / 50 mL in 1 BAG (0409-7101-68)", "package_ndc": "0409-7101-66", "marketing_start_date": "20050719"}, {"sample": false, "description": "10 POUCH in 1 CASE (0409-7101-67)  / 5 BAG in 1 POUCH / 100 mL in 1 BAG (0409-7101-69)", "package_ndc": "0409-7101-67", "marketing_start_date": "20050824"}], "brand_name": "Sodium Chloride", "product_id": "0409-7101_f233e72c-072d-4a43-857a-f4d5791e1a73", "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": "0409-7101", "generic_name": "Sodium Chloride", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Chloride", "active_ingredients": [{"name": "SODIUM CHLORIDE", "strength": "900 mg/100mL"}], "application_number": "NDA019465", "marketing_category": "NDA", "marketing_start_date": "20050630", "listing_expiration_date": "20271231"}