Package 65219-282-10
Brand: sodium chloride
Generic: sodium chloridePackage Facts
Identity
Package NDC
65219-282-10
Digits Only
6521928210
Product NDC
65219-282
Description
10 BAG in 1 CASE (65219-282-10) / 1000 mL in 1 BAG (65219-282-01)
Marketing
Marketing Status
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": "2ad355c8-4420-42d5-8ea8-b4cc3ccc1c0e", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["1807639"], "spl_set_id": ["6d43fa91-0940-437f-ba70-b2d3f977593e"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BAG in 1 CASE (65219-282-10) / 1000 mL in 1 BAG (65219-282-01)", "package_ndc": "65219-282-10", "marketing_start_date": "20230630"}], "brand_name": "Sodium chloride", "product_id": "65219-282_2ad355c8-4420-42d5-8ea8-b4cc3ccc1c0e", "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": "65219-282", "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": "20230630", "listing_expiration_date": "20261231"}