Package 42291-506-50

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 42291-506-50
Digits Only 4229150650
Product NDC 42291-506
Product ID 42291-506_3a9ee76a-b914-17bb-e063-6294a90aad71
Description

500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42291-506-50)

Marketing

Marketing Status
Marketed Since 2019-06-21
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": "3a9ee76a-b914-17bb-e063-6294a90aad71", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["628953"], "spl_set_id": ["8bb030b7-104a-373b-e053-2995a90ab580"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42291-506-01)", "package_ndc": "42291-506-01", "marketing_start_date": "20190621"}, {"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42291-506-50)", "package_ndc": "42291-506-50", "marketing_start_date": "20190621"}], "brand_name": "Potassium Chloride", "product_id": "42291-506_3a9ee76a-b914-17bb-e063-6294a90aad71", "dosage_form": "TABLET, FILM COATED, 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": "42291-506", "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": "NDA019123", "marketing_category": "NDA", "marketing_start_date": "20190621", "listing_expiration_date": "20261231"}