bacteriostatic sodium chloride

Generic: sodium chloride

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

Drug Facts

Product Profile

Brand Name bacteriostatic 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 0409-1966
Product ID 0409-1966_2d3125e0-c89b-46d5-a350-07d1e7936ebd
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA018800
Listing Expiration 2026-12-31
Marketing Start 2005-04-30

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04091966
Hyphenated Format 0409-1966

Supplemental Identifiers

RxCUI
313002
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 bacteriostatic sodium chloride (source: ndc)
Generic Name sodium chloride (source: ndc)
Application Number NDA018800 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 9 mg/mL
source: ndc
Packaging
  • 25 VIAL, MULTI-DOSE in 1 TRAY (0409-1966-05) / 20 mL in 1 VIAL, MULTI-DOSE (0409-1966-01)
  • 25 VIAL, MULTI-DOSE in 1 TRAY (0409-1966-07) / 30 mL in 1 VIAL, MULTI-DOSE (0409-1966-02)
  • 25 VIAL, MULTI-DOSE in 1 TRAY (0409-1966-12) / 10 mL in 1 VIAL, MULTI-DOSE (0409-1966-06)
source: ndc

Packages (3)

0409-1966-05 25 VIAL, MULTI-DOSE in 1 TRAY (0409-1966-05) / 20 mL in 1 VIAL, MULTI-DOSE (0409-1966-01) 0409-1966-07 25 VIAL, MULTI-DOSE in 1 TRAY (0409-1966-07) / 30 mL in 1 VIAL, MULTI-DOSE (0409-1966-02) 0409-1966-12 25 VIAL, MULTI-DOSE in 1 TRAY (0409-1966-12) / 10 mL in 1 VIAL, MULTI-DOSE (0409-1966-06)

Ingredients (1)

sodium chloride (9 mg/mL)

Linked Drug Pages (1)

BACTERIOSTATIC SODIUM CHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "2d3125e0-c89b-46d5-a350-07d1e7936ebd", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["313002"], "spl_set_id": ["376093e7-e09e-4a57-3199-195e45251866"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, MULTI-DOSE in 1 TRAY (0409-1966-05)  / 20 mL in 1 VIAL, MULTI-DOSE (0409-1966-01)", "package_ndc": "0409-1966-05", "marketing_start_date": "20050502"}, {"sample": false, "description": "25 VIAL, MULTI-DOSE in 1 TRAY (0409-1966-07)  / 30 mL in 1 VIAL, MULTI-DOSE (0409-1966-02)", "package_ndc": "0409-1966-07", "marketing_start_date": "20050430"}, {"sample": false, "description": "25 VIAL, MULTI-DOSE in 1 TRAY (0409-1966-12)  / 10 mL in 1 VIAL, MULTI-DOSE (0409-1966-06)", "package_ndc": "0409-1966-12", "marketing_start_date": "20051007"}], "brand_name": "BACTERIOSTATIC SODIUM CHLORIDE", "product_id": "0409-1966_2d3125e0-c89b-46d5-a350-07d1e7936ebd", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "0409-1966", "generic_name": "SODIUM CHLORIDE", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BACTERIOSTATIC SODIUM CHLORIDE", "active_ingredients": [{"name": "SODIUM CHLORIDE", "strength": "9 mg/mL"}], "application_number": "NDA018800", "marketing_category": "NDA", "marketing_start_date": "20050430", "listing_expiration_date": "20261231"}