Package 72789-365-82

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 72789-365-82
Digits Only 7278936582
Product NDC 72789-365
Description

500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-365-82)

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": "3ba1064c-b041-c2b7-e063-6394a90ad3ce", "openfda": {"upc": ["0372789365305"], "unii": ["660YQ98I10"], "rxcui": ["1801294"], "spl_set_id": ["47a87fb6-5e61-41c9-b759-10f7c74a67ce"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-365-01)", "package_ndc": "72789-365-01", "marketing_start_date": "20231204"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-365-30)", "package_ndc": "72789-365-30", "marketing_start_date": "20231228"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-365-60)", "package_ndc": "72789-365-60", "marketing_start_date": "20240119"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-365-82)", "package_ndc": "72789-365-82", "marketing_start_date": "20231114"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-365-90)", "package_ndc": "72789-365-90", "marketing_start_date": "20240119"}, {"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-365-95)", "package_ndc": "72789-365-95", "marketing_start_date": "20231228"}], "brand_name": "Potassium Chloride", "product_id": "72789-365_3ba1064c-b041-c2b7-e063-6394a90ad3ce", "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": "72789-365", "generic_name": "Potassium Chloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "20 meq/1"}], "application_number": "ANDA076368", "marketing_category": "ANDA", "marketing_start_date": "20231114", "listing_expiration_date": "20261231"}