Package 0409-4888-20

Brand: sodium chloride

Generic: sodium chloride
NDC Package

Package Facts

Identity

Package NDC 0409-4888-20
Digits Only 0409488820
Product NDC 0409-4888
Product ID 0409-4888_9ee88abb-024a-4a3b-9776-1777eaf2f760
Description

25 VIAL, SINGLE-DOSE in 1 TRAY (0409-4888-20) / 20 mL in 1 VIAL, SINGLE-DOSE (0409-4888-03)

Marketing

Marketing Status
Marketed Since 2005-02-28
Brand sodium chloride
Generic sodium chloride
Sample Package No

Linked Drug Pages (1)

Sodium Chloride ndc-match (0.95)

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"}