Package 67046-1589-3

Brand: furosemide

Generic: furosemide
NDC Package

Package Facts

Identity

Package NDC 67046-1589-3
Digits Only 6704615893
Product NDC 67046-1589
Description

30 TABLET in 1 BLISTER PACK (67046-1589-3)

Marketing

Marketing Status
Marketed Since 2025-09-16
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": "3eed4b0a-4a37-7442-e063-6294a90a3306", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["310429"], "spl_set_id": ["3eed4bbf-7d0e-e852-e063-6394a90a85c2"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (67046-1589-3)", "package_ndc": "67046-1589-3", "marketing_start_date": "20250916"}], "brand_name": "Furosemide", "product_id": "67046-1589_3eed4b0a-4a37-7442-e063-6294a90a3306", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "67046-1589", "generic_name": "Furosemide", "labeler_name": "Coupler LLC", "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": "20250916", "listing_expiration_date": "20261231"}