Package 67046-1555-3
Brand: furosemide
Generic: furosemidePackage Facts
Identity
Package NDC
67046-1555-3
Digits Only
6704615553
Product NDC
67046-1555
Description
30 TABLET in 1 BLISTER PACK (67046-1555-3)
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": "33ec714c-3600-62f6-e063-6394a90afee9", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["197732"], "spl_set_id": ["33ec71e2-8fbd-0703-e063-6294a90a62e1"], "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 (67046-1555-3)", "package_ndc": "67046-1555-3", "marketing_start_date": "20250429"}], "brand_name": "Furosemide", "product_id": "67046-1555_33ec714c-3600-62f6-e063-6394a90afee9", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "67046-1555", "generic_name": "Furosemide", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "80 mg/1"}], "application_number": "ANDA077293", "marketing_category": "ANDA", "marketing_start_date": "20250429", "listing_expiration_date": "20261231"}