Package 63629-2620-4
Brand: potassium chloride
Generic: potassium chloridePackage Facts
Identity
Package NDC
63629-2620-4
Digits Only
6362926204
Product NDC
63629-2620
Description
180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2620-4)
Marketing
Marketing Status
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": "969312e9-8b4a-4f3a-823d-903600206b47", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["312529"], "spl_set_id": ["9088ca44-5585-4551-8e2c-168f306520d4"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2620-1)", "package_ndc": "63629-2620-1", "marketing_start_date": "20240206"}, {"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2620-2)", "package_ndc": "63629-2620-2", "marketing_start_date": "20240206"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2620-3)", "package_ndc": "63629-2620-3", "marketing_start_date": "20240206"}, {"sample": false, "description": "180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2620-4)", "package_ndc": "63629-2620-4", "marketing_start_date": "20240206"}, {"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2620-5)", "package_ndc": "63629-2620-5", "marketing_start_date": "20240206"}], "brand_name": "Potassium Chloride", "product_id": "63629-2620_969312e9-8b4a-4f3a-823d-903600206b47", "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": "63629-2620", "generic_name": "Potassium Chloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "600 mg/1"}], "application_number": "ANDA210921", "marketing_category": "ANDA", "marketing_start_date": "20181219", "listing_expiration_date": "20261231"}