furosemide

Generic: furosemide

Labeler: leading pharma, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name furosemide
Generic Name furosemide
Labeler leading pharma, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

furosemide 80 mg/1

Manufacturer
Leading Pharma, LLC

Identifiers & Regulatory

Product NDC 69315-118
Product ID 69315-118_445bfa17-a52c-4492-9dbc-94218b30c1db
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077293
Listing Expiration 2026-12-31
Marketing Start 2006-02-01

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 69315118
Hyphenated Format 69315-118

Supplemental Identifiers

RxCUI
197732 310429 313988
UNII
7LXU5N7ZO5
NUI
N0000175366 N0000175590

Packaging Origin

Original Packager
true

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 ANDA077293 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 80 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (69315-118-01)
  • 500 TABLET in 1 BOTTLE (69315-118-05)
source: ndc

Packages (2)

69315-118-01 100 TABLET in 1 BOTTLE (69315-118-01) 69315-118-05 500 TABLET in 1 BOTTLE (69315-118-05)

Ingredients (1)

furosemide (80 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": "445bfa17-a52c-4492-9dbc-94218b30c1db", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["197732", "310429", "313988"], "spl_set_id": ["b5c6fcf4-fd37-4fee-8dac-1a3273d95ffe"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Leading Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69315-118-01)", "package_ndc": "69315-118-01", "marketing_start_date": "20160515"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (69315-118-05)", "package_ndc": "69315-118-05", "marketing_start_date": "20160515"}], "brand_name": "Furosemide", "product_id": "69315-118_445bfa17-a52c-4492-9dbc-94218b30c1db", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "69315-118", "generic_name": "Furosemide", "labeler_name": "Leading Pharma, 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": "20060201", "listing_expiration_date": "20261231"}