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
INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
Active Ingredients

sodium chloride 9 mg/mL

Manufacturer
Hospira, Inc.

Identifiers & Regulatory

Product NDC 0409-4888
Product ID 0409-4888_9ee88abb-024a-4a3b-9776-1777eaf2f760
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA018803
Listing Expiration 2026-12-31
Marketing Start 2005-02-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04094888
Hyphenated Format 0409-4888

Supplemental Identifiers

RxCUI
1807628 1807631 1807637 1807638
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 NDA018803 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 9 mg/mL
source: ndc
Packaging
  • 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-4888-10) / 10 mL in 1 VIAL, SINGLE-DOSE (0409-4888-02)
  • 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-4888-12) / 10 mL in 1 VIAL, SINGLE-DOSE (0409-4888-01)
  • 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-4888-20) / 20 mL in 1 VIAL, SINGLE-DOSE (0409-4888-03)
  • 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-4888-50) / 50 mL in 1 VIAL, SINGLE-DOSE (0409-4888-06)
  • 10 VIAL, SINGLE-DOSE in 1 TRAY (0409-4888-90) / 10 mL in 1 VIAL, SINGLE-DOSE (0409-4888-02)
source: ndc

Packages (5)

0409-4888-10 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-4888-10) / 10 mL in 1 VIAL, SINGLE-DOSE (0409-4888-02) 0409-4888-12 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-4888-12) / 10 mL in 1 VIAL, SINGLE-DOSE (0409-4888-01) 0409-4888-20 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-4888-20) / 20 mL in 1 VIAL, SINGLE-DOSE (0409-4888-03) 0409-4888-50 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-4888-50) / 50 mL in 1 VIAL, SINGLE-DOSE (0409-4888-06) 0409-4888-90 10 VIAL, SINGLE-DOSE in 1 TRAY (0409-4888-90) / 10 mL in 1 VIAL, SINGLE-DOSE (0409-4888-02)

Ingredients (1)

sodium chloride (9 mg/mL)

Linked Drug Pages (1)

Sodium Chloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "9ee88abb-024a-4a3b-9776-1777eaf2f760", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["1807628", "1807631", "1807637", "1807638"], "spl_set_id": ["8eb172da-dcd4-4660-4a8f-ad44a14b4af7"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 TRAY (0409-4888-10)  / 10 mL in 1 VIAL, SINGLE-DOSE (0409-4888-02)", "package_ndc": "0409-4888-10", "marketing_start_date": "20050430"}, {"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 TRAY (0409-4888-12)  / 10 mL in 1 VIAL, SINGLE-DOSE (0409-4888-01)", "package_ndc": "0409-4888-12", "marketing_start_date": "20050714"}, {"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 TRAY (0409-4888-20)  / 20 mL in 1 VIAL, SINGLE-DOSE (0409-4888-03)", "package_ndc": "0409-4888-20", "marketing_start_date": "20050228"}, {"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 TRAY (0409-4888-50)  / 50 mL in 1 VIAL, SINGLE-DOSE (0409-4888-06)", "package_ndc": "0409-4888-50", "marketing_start_date": "20050228"}, {"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 TRAY (0409-4888-90)  / 10 mL in 1 VIAL, SINGLE-DOSE (0409-4888-02)", "package_ndc": "0409-4888-90", "marketing_start_date": "20211020"}], "brand_name": "Sodium Chloride", "product_id": "0409-4888_9ee88abb-024a-4a3b-9776-1777eaf2f760", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "0409-4888", "generic_name": "Sodium Chloride", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Chloride", "active_ingredients": [{"name": "SODIUM CHLORIDE", "strength": "9 mg/mL"}], "application_number": "NDA018803", "marketing_category": "NDA", "marketing_start_date": "20050228", "listing_expiration_date": "20261231"}