Package 65219-502-10

Brand: sodium chloride

Generic: sodium chloride
NDC Package

Package Facts

Identity

Package NDC 65219-502-10
Digits Only 6521950210
Product NDC 65219-502
Description

6 BAG in 1 CASE (65219-502-10) / 1000 mL in 1 BAG (65219-502-01)

Marketing

Marketing Status
Marketed Since 2025-12-19
Brand sodium chloride
Generic sodium chloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["IRRIGATION"], "spl_id": "53843388-e3bc-4344-87aa-b345680ec27b", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["486515"], "spl_set_id": ["ce0c8c6f-734a-400f-9b60-a3b1e263f25f"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 BAG in 1 CASE (65219-502-10)  / 1000 mL in 1 BAG (65219-502-01)", "package_ndc": "65219-502-10", "marketing_start_date": "20251219"}], "brand_name": "Sodium chloride", "product_id": "65219-502_53843388-e3bc-4344-87aa-b345680ec27b", "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": "65219-502", "generic_name": "SODIUM CHLORIDE", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium chloride", "active_ingredients": [{"name": "SODIUM CHLORIDE", "strength": ".9 g/100mL"}], "application_number": "ANDA213688", "marketing_category": "ANDA", "marketing_start_date": "20251219", "listing_expiration_date": "20261231"}