Package 70518-2528-1
Brand: furosemide
Generic: furosemidePackage Facts
Identity
Package NDC
70518-2528-1
Digits Only
7051825281
Product NDC
70518-2528
Description
30 TABLET in 1 BLISTER PACK (70518-2528-1)
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": "4a659a58-7fb2-57c1-e063-6394a90a4537", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["310429"], "spl_set_id": ["7cdcd001-ab4b-4210-a455-2e17a7bc4972"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-2528-1)", "package_ndc": "70518-2528-1", "marketing_start_date": "20250821"}], "brand_name": "Furosemide", "product_id": "70518-2528_4a659a58-7fb2-57c1-e063-6394a90a4537", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "70518-2528", "generic_name": "Furosemide", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "20 mg/1"}], "application_number": "ANDA077293", "marketing_category": "ANDA", "marketing_start_date": "20200107", "listing_expiration_date": "20271231"}