furosemide

Generic: furosemide

Labeler: cardinal health 107, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name furosemide
Generic Name furosemide
Labeler cardinal health 107, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

furosemide 20 mg/1

Manufacturer
Cardinal Health 107, LLC

Identifiers & Regulatory

Product NDC 55154-2349
Product ID 55154-2349_392096c5-3e3f-47c0-b793-54392f17ccf8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076796
Listing Expiration 2026-12-31
Marketing Start 2024-12-04

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 551542349
Hyphenated Format 55154-2349

Supplemental Identifiers

RxCUI
310429 313988
UPC
0055154234900 0055154234801
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 ANDA076796 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 10 BLISTER PACK in 1 BAG (55154-2349-0) / 1 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

55154-2349-0 10 BLISTER PACK in 1 BAG (55154-2349-0) / 1 TABLET in 1 BLISTER PACK

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": "392096c5-3e3f-47c0-b793-54392f17ccf8", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0055154234900", "0055154234801"], "unii": ["7LXU5N7ZO5"], "rxcui": ["310429", "313988"], "spl_set_id": ["2a5bcf50-6d63-463a-915e-a72ea2e5f131"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BAG (55154-2349-0)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "55154-2349-0", "marketing_start_date": "20241204"}], "brand_name": "Furosemide", "product_id": "55154-2349_392096c5-3e3f-47c0-b793-54392f17ccf8", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "55154-2349", "generic_name": "furosemide", "labeler_name": "Cardinal Health 107, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "20 mg/1"}], "application_number": "ANDA076796", "marketing_category": "ANDA", "marketing_start_date": "20241204", "listing_expiration_date": "20261231"}