Package 72865-195-05

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 72865-195-05
Digits Only 7286519505
Product NDC 72865-195
Description

500 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-195-05)

Marketing

Marketing Status
Marketed Since 2021-03-04
Brand potassium chloride
Generic potassium chloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "32424946-c3ae-434b-844c-5b4cdb1f605e", "openfda": {"upc": ["0372865196014", "0372865196052", "0372865195017", "0372865195055", "0372865194010", "0372865194058"], "unii": ["660YQ98I10"], "rxcui": ["403888", "1801294", "1801298"], "spl_set_id": ["7fd82f08-8ad0-4ee2-8eb6-5c973f98baee"], "manufacturer_name": ["XLCare Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-195-01)", "package_ndc": "72865-195-01", "marketing_start_date": "20210304"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-195-05)", "package_ndc": "72865-195-05", "marketing_start_date": "20210304"}], "brand_name": "POTASSIUM CHLORIDE", "product_id": "72865-195_32424946-c3ae-434b-844c-5b4cdb1f605e", "dosage_form": "TABLET, EXTENDED RELEASE", "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": "72865-195", "generic_name": "Potassium Chloride", "labeler_name": "XLCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "POTASSIUM CHLORIDE", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1125 mg/1"}], "application_number": "ANDA214422", "marketing_category": "ANDA", "marketing_start_date": "20210304", "listing_expiration_date": "20261231"}