Package 69315-118-05
Brand: furosemide
Generic: furosemidePackage Facts
Identity
Package NDC
69315-118-05
Digits Only
6931511805
Product NDC
69315-118
Description
500 TABLET in 1 BOTTLE (69315-118-05)
Marketing
Marketing Status
Brand
furosemide
Generic
furosemide
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "445bfa17-a52c-4492-9dbc-94218b30c1db", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["197732", "310429", "313988"], "spl_set_id": ["b5c6fcf4-fd37-4fee-8dac-1a3273d95ffe"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Leading Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69315-118-01)", "package_ndc": "69315-118-01", "marketing_start_date": "20160515"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (69315-118-05)", "package_ndc": "69315-118-05", "marketing_start_date": "20160515"}], "brand_name": "Furosemide", "product_id": "69315-118_445bfa17-a52c-4492-9dbc-94218b30c1db", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "69315-118", "generic_name": "Furosemide", "labeler_name": "Leading Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "80 mg/1"}], "application_number": "ANDA077293", "marketing_category": "ANDA", "marketing_start_date": "20060201", "listing_expiration_date": "20261231"}