Package 82868-027-90

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 82868-027-90
Digits Only 8286802790
Product NDC 82868-027
Description

90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-027-90)

Marketing

Marketing Status
Marketed Since 2023-11-14
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": "46dc8f32-692b-a243-e063-6394a90a19f8", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["1801298"], "spl_set_id": ["0a72cc27-e092-d85a-e063-6294a90a503c"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-027-90)", "package_ndc": "82868-027-90", "marketing_start_date": "20231114"}], "brand_name": "Potassium Chloride", "product_id": "82868-027_46dc8f32-692b-a243-e063-6394a90a19f8", "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": "82868-027", "generic_name": "potassium chloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA074726", "marketing_category": "ANDA", "marketing_start_date": "20231114", "listing_expiration_date": "20261231"}