Package 0409-1141-02

Brand: sodium chloride

Generic: sodium chloride
NDC Package

Package Facts

Identity

Package NDC 0409-1141-02
Digits Only 0409114102
Product NDC 0409-1141
Product ID 0409-1141_4b8e6f49-4268-4654-9b7d-8dcd235aa040
Description

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

Marketing

Marketing Status
Marketed Since 2005-04-30
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": ["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"}