Package 50090-7708-0

Brand: furosemide

Generic: furosemide
NDC Package

Package Facts

Identity

Package NDC 50090-7708-0
Digits Only 5009077080
Product NDC 50090-7708
Description

90 TABLET in 1 BOTTLE (50090-7708-0)

Marketing

Marketing Status
Marketed Since 2025-10-14
Brand furosemide
Generic furosemide
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "173fff1a-9e08-4d83-aa75-75606a80f2cf", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["310429"], "spl_set_id": ["3f3248cd-d62f-49ca-8788-f059e8facd91"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7708-0)", "package_ndc": "50090-7708-0", "marketing_start_date": "20251014"}], "brand_name": "Furosemide", "product_id": "50090-7708_173fff1a-9e08-4d83-aa75-75606a80f2cf", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "50090-7708", "generic_name": "Furosemide", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "20 mg/1"}], "application_number": "ANDA078010", "marketing_category": "ANDA", "marketing_start_date": "20240603", "listing_expiration_date": "20261231"}