Package 65219-222-25
Brand: sodium chloride
Generic: sodium chloridePackage Facts
Identity
Package NDC
65219-222-25
Digits Only
6521922225
Product NDC
65219-222
Description
30 BAG in 1 CASE (65219-222-25) / 250 mL in 1 BAG (65219-222-01)
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": "d5c0c612-d7b8-458f-8ad3-d3999b3bd89d", "openfda": {"unii": ["451W47IQ8X"], "rxcui": ["1807631", "1807632", "1807633", "1807634"], "spl_set_id": ["d98bf9f7-30ec-4927-a577-cabad192cb18"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 BAG in 1 CASE (65219-222-25) / 250 mL in 1 BAG (65219-222-01)", "package_ndc": "65219-222-25", "marketing_start_date": "20211117"}], "brand_name": "Sodium chloride", "product_id": "65219-222_d5c0c612-d7b8-458f-8ad3-d3999b3bd89d", "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": "65219-222", "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": "20271231"}