furosemide

Generic: furosemide

Labeler: coupler llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name furosemide
Generic Name furosemide
Labeler coupler llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

furosemide 20 mg/1

Manufacturer
Coupler LLC

Identifiers & Regulatory

Product NDC 67046-1589
Product ID 67046-1589_3eed4b0a-4a37-7442-e063-6294a90a3306
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078010
Listing Expiration 2026-12-31
Marketing Start 2025-09-16

Pharmacologic Class

Established (EPC)
loop diuretic [epc]
Physiologic Effect
increased diuresis at loop of henle [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 670461589
Hyphenated Format 67046-1589

Supplemental Identifiers

RxCUI
310429
UNII
7LXU5N7ZO5
NUI
N0000175366 N0000175590

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name furosemide (source: ndc)
Generic Name furosemide (source: ndc)
Application Number ANDA078010 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BLISTER PACK (67046-1589-3)
source: ndc

Packages (1)

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

Ingredients (1)

furosemide (20 mg/1)

Linked Drug Pages (1)

Furosemide ndc-match (0.9)

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"}