Package 59651-431-05
Brand: potassium chloride
Generic: potassium chloridePackage Facts
Identity
Package NDC
59651-431-05
Digits Only
5965143105
Product NDC
59651-431
Description
500 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-431-05)
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": "d1038d80-ef7d-456a-9f47-0c5df1ca8811", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["403888", "1801294", "1801298"], "spl_set_id": ["deb6b462-397f-4527-ae26-40dc5d5857bc"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-431-01)", "package_ndc": "59651-431-01", "marketing_start_date": "20210331"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-431-05)", "package_ndc": "59651-431-05", "marketing_start_date": "20210331"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-431-90)", "package_ndc": "59651-431-90", "marketing_start_date": "20210331"}], "brand_name": "Potassium Chloride", "product_id": "59651-431_d1038d80-ef7d-456a-9f47-0c5df1ca8811", "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": "59651-431", "generic_name": "Potassium Chloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "1500 mg/1"}], "application_number": "ANDA214728", "marketing_category": "ANDA", "marketing_start_date": "20210331", "listing_expiration_date": "20261231"}