Package 65219-512-50

Brand: potassium acetate

Generic: potassium acetate
NDC Package

Package Facts

Identity

Package NDC 65219-512-50
Digits Only 6521951250
Product NDC 65219-512
Product ID 65219-512_ea996741-0733-42bc-9ea6-4392cbfb2c37
Description

25 VIAL, PHARMACY BULK PACKAGE in 1 TRAY (65219-512-50) / 50 mL in 1 VIAL, PHARMACY BULK PACKAGE (65219-512-02)

Marketing

Marketing Status
Marketed Since 2024-11-27
Brand potassium acetate
Generic potassium acetate
Sample Package No

Linked Drug Pages (1)

Potassium Acetate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "ea996741-0733-42bc-9ea6-4392cbfb2c37", "openfda": {"upc": ["0365219512028"], "unii": ["M911911U02"], "rxcui": ["237381"], "spl_set_id": ["2f069f41-903a-4a57-b566-eda5c44367d8"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, PHARMACY BULK PACKAGE in 1 TRAY (65219-512-50)  / 50 mL in 1 VIAL, PHARMACY BULK PACKAGE (65219-512-02)", "package_ndc": "65219-512-50", "marketing_start_date": "20241127"}], "brand_name": "Potassium Acetate", "product_id": "65219-512_ea996741-0733-42bc-9ea6-4392cbfb2c37", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Potassium Compounds [CS]", "Potassium Salt [EPC]"], "product_ndc": "65219-512", "generic_name": "POTASSIUM ACETATE", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Acetate", "active_ingredients": [{"name": "POTASSIUM ACETATE", "strength": "196 mg/mL"}], "application_number": "ANDA217515", "marketing_category": "ANDA", "marketing_start_date": "20241127", "listing_expiration_date": "20261231"}