Package 17224-185-21
Brand: furosemide
Generic: furosemidePackage Facts
Identity
Package NDC
17224-185-21
Digits Only
1722418521
Product NDC
17224-185
Description
21 TABLET in 1 BOTTLE, PLASTIC (17224-185-21)
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": "166340cd-364a-14fd-e063-6294a90a03b4", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["313988"], "spl_set_id": ["b2cc89e5-6619-4113-ad31-48076652c856"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Calvin Scott & Co., Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET in 1 BOTTLE, PLASTIC (17224-185-21)", "package_ndc": "17224-185-21", "marketing_start_date": "20160515"}], "brand_name": "Furosemide", "product_id": "17224-185_166340cd-364a-14fd-e063-6294a90a03b4", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "17224-185", "generic_name": "FUROSEMIDE", "labeler_name": "Calvin Scott & Co., Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "40 mg/1"}], "application_number": "ANDA077293", "marketing_category": "ANDA", "marketing_start_date": "20060201", "listing_expiration_date": "20261231"}