Package 42291-487-01

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 42291-487-01
Digits Only 4229148701
Product NDC 42291-487
Product ID 42291-487_3bdfceef-6db4-8d5d-e063-6294a90abecc
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (42291-487-01)

Marketing

Marketing Status
Marketed Since 2025-08-08
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": ["ORAL"], "spl_id": "3bdfceef-6db4-8d5d-e063-6294a90abecc", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["628953"], "spl_set_id": ["3bdfced1-6e62-9e92-e063-6294a90a28aa"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (42291-487-01)", "package_ndc": "42291-487-01", "marketing_start_date": "20250808"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (42291-487-50)", "package_ndc": "42291-487-50", "marketing_start_date": "20250808"}], "brand_name": "Potassium Chloride", "product_id": "42291-487_3bdfceef-6db4-8d5d-e063-6294a90abecc", "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": "42291-487", "generic_name": "Potassium Chloride", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA218979", "marketing_category": "ANDA", "marketing_start_date": "20250808", "listing_expiration_date": "20261231"}