Package 65219-004-01

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 65219-004-01
Digits Only 6521900401
Product NDC 65219-004
Product ID 65219-004_771b8cdf-5287-4678-af79-7dc0c78245cc
Description

60 BAG in 1 CARTON (65219-004-01) / 50 mL in 1 BAG (65219-004-00)

Marketing

Marketing Status
Marketed Since 2021-06-25
Brand potassium chloride
Generic potassium chloride
Sample Package No

Linked Drug Pages (1)

POTASSIUM CHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "771b8cdf-5287-4678-af79-7dc0c78245cc", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["312507", "1860239", "1860241", "1860463", "1860466"], "spl_set_id": ["3849b89c-c309-46fb-a1e2-53ff0c65077f"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 BAG in 1 CARTON (65219-004-01)  / 50 mL in 1 BAG (65219-004-00)", "package_ndc": "65219-004-01", "marketing_start_date": "20210625"}], "brand_name": "POTASSIUM CHLORIDE", "product_id": "65219-004_771b8cdf-5287-4678-af79-7dc0c78245cc", "dosage_form": "INJECTION", "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": "65219-004", "generic_name": "POTASSIUM CHLORIDE", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CHLORIDE", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "10 meq/50mL"}], "application_number": "ANDA211087", "marketing_category": "ANDA", "marketing_start_date": "20210625", "listing_expiration_date": "20261231"}