Package 65219-510-20

Brand: potassium acetate

Generic: potassium acetate
NDC Package

Package Facts

Identity

Package NDC 65219-510-20
Digits Only 6521951020
Product NDC 65219-510
Product ID 65219-510_67c83f58-73cd-47d2-8dbc-e0fd8331c6e7
Description

25 VIAL, SINGLE-DOSE in 1 TRAY (65219-510-20) / 20 mL in 1 VIAL, SINGLE-DOSE (65219-510-02)

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": "67c83f58-73cd-47d2-8dbc-e0fd8331c6e7", "openfda": {"upc": ["0365219510024"], "unii": ["M911911U02"], "rxcui": ["1871155"], "spl_set_id": ["bf4dc488-d6f3-41f8-ac8d-37b27f25b8db"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 TRAY (65219-510-20)  / 20 mL in 1 VIAL, SINGLE-DOSE (65219-510-02)", "package_ndc": "65219-510-20", "marketing_start_date": "20241127"}], "brand_name": "Potassium Acetate", "product_id": "65219-510_67c83f58-73cd-47d2-8dbc-e0fd8331c6e7", "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": "65219-510", "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": "3.93 g/20mL"}], "application_number": "ANDA217515", "marketing_category": "ANDA", "marketing_start_date": "20241127", "listing_expiration_date": "20261231"}