Package 65219-232-50

Brand: sodium chloride

Generic: sodium chloride
NDC Package

Package Facts

Identity

Package NDC 65219-232-50
Digits Only 6521923250
Product NDC 65219-232
Product ID 65219-232_02cd6592-b609-44d9-9fb3-3fb077e9a4fb
Description

20 BAG in 1 CASE (65219-232-50) / 500 mL in 1 BAG (65219-232-01)

Marketing

Marketing Status
Marketed Since 2021-11-30
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": "02cd6592-b609-44d9-9fb3-3fb077e9a4fb", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["1807548", "1807549", "1807550", "1807551"], "spl_set_id": ["239a5af1-7498-480f-862c-ab7c3d89d183"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 BAG in 1 CASE (65219-232-50)  / 500 mL in 1 BAG (65219-232-01)", "package_ndc": "65219-232-50", "marketing_start_date": "20211130"}], "brand_name": "Sodium chloride", "product_id": "65219-232_02cd6592-b609-44d9-9fb3-3fb077e9a4fb", "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": "65219-232", "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": "2250 mg/500mL"}], "application_number": "ANDA208122", "marketing_category": "ANDA", "marketing_start_date": "20180723", "listing_expiration_date": "20261231"}