Package 84549-251-25

Brand: furosemide

Generic: furosemide
NDC Package

Package Facts

Identity

Package NDC 84549-251-25
Digits Only 8454925125
Product NDC 84549-251
Description

4 mL in 1 VIAL (84549-251-25)

Marketing

Marketing Status
Marketed Since 2025-08-27
Brand furosemide
Generic furosemide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "463ce3e6-a666-9db5-e063-6394a90a91ee", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["1719291"], "spl_set_id": ["38550de1-f099-0cdf-e063-6294a90a9e26"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "4 mL in 1 VIAL (84549-251-25)", "package_ndc": "84549-251-25", "marketing_start_date": "20250827"}], "brand_name": "Furosemide", "product_id": "84549-251_463ce3e6-a666-9db5-e063-6394a90a91ee", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "84549-251", "generic_name": "Furosemide", "labeler_name": "ProPharma Distribution", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "10 mg/mL"}], "application_number": "ANDA203428", "marketing_category": "ANDA", "marketing_start_date": "20230201", "listing_expiration_date": "20261231"}