Package 62037-560-10
Brand: potassium chloride
Generic: potassium chloridePackage Facts
Identity
Package NDC
62037-560-10
Digits Only
6203756010
Product NDC
62037-560
Description
1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-560-10)
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": "57df625b-891f-4826-a64b-46db5e64378e", "openfda": {"upc": ["0362037560903"], "unii": ["660YQ98I10"], "rxcui": ["312504", "315183"], "spl_set_id": ["ed5baaf6-270b-4dd3-b100-36030c0098fc"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-560-01)", "package_ndc": "62037-560-01", "marketing_end_date": "20261031", "marketing_start_date": "20080825"}, {"sample": false, "description": "500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-560-05)", "package_ndc": "62037-560-05", "marketing_end_date": "20261031", "marketing_start_date": "20080825"}, {"sample": false, "description": "1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-560-10)", "package_ndc": "62037-560-10", "marketing_end_date": "20261031", "marketing_start_date": "20080825"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-560-90)", "package_ndc": "62037-560-90", "marketing_end_date": "20260531", "marketing_start_date": "20080825"}], "brand_name": "Potassium Chloride", "product_id": "62037-560_57df625b-891f-4826-a64b-46db5e64378e", "dosage_form": "CAPSULE, 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": "62037-560", "generic_name": "Potassium Chloride", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA077419", "marketing_category": "ANDA", "marketing_end_date": "20261031", "marketing_start_date": "20080825"}