Package 65219-328-50

Brand: sodium chloride

Generic: sodium chloride
NDC Package

Package Facts

Identity

Package NDC 65219-328-50
Digits Only 6521932850
Product NDC 65219-328
Description

10 BAG in 1 CASE (65219-328-50) / 1000 mL in 1 BAG (65219-328-10)

Marketing

Marketing Status
Marketed Since 2023-09-11
Brand sodium chloride
Generic sodium chloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "904e72e0-2558-4548-8ddd-8c6877c23b98", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["1807634", "1807639"], "spl_set_id": ["2e5fe9f4-78e5-4af4-8bf9-9680e5dc5e88"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BAG in 1 CASE (65219-328-50)  / 1000 mL in 1 BAG (65219-328-10)", "package_ndc": "65219-328-50", "marketing_start_date": "20230911"}], "brand_name": "Sodium Chloride", "product_id": "65219-328_904e72e0-2558-4548-8ddd-8c6877c23b98", "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": "65219-328", "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 mg/mL"}], "application_number": "ANDA207310", "marketing_category": "ANDA", "marketing_start_date": "20170919", "listing_expiration_date": "20261231"}