Package 0054-4301-25
Brand: furosemide
Generic: furosemidePackage Facts
Identity
Package NDC
0054-4301-25
Digits Only
0054430125
Product NDC
0054-4301
Description
100 TABLET in 1 BOTTLE, PLASTIC (0054-4301-25)
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": "bc62ddda-7639-4090-99f0-7dd4d13518f3", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0300544301251", "0300544299251", "0300544297257", "0300543298637"], "unii": ["7LXU5N7ZO5"], "rxcui": ["197730", "197731", "197732", "310429", "313988"], "spl_set_id": ["9e493331-dddd-496e-abf8-61747fb67aba"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (0054-4301-25)", "package_ndc": "0054-4301-25", "marketing_start_date": "19910313"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (0054-4301-29)", "package_ndc": "0054-4301-29", "marketing_start_date": "19910313"}], "brand_name": "Furosemide", "product_id": "0054-4301_bc62ddda-7639-4090-99f0-7dd4d13518f3", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "0054-4301", "generic_name": "Furosemide", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "80 mg/1"}], "application_number": "ANDA070086", "marketing_category": "ANDA", "marketing_start_date": "19910313", "listing_expiration_date": "20271231"}