furosemide

Generic: furosemide

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name furosemide
Generic Name furosemide
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

furosemide 20 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 63187-739
Product ID 63187-739_7a15b0c4-de78-4bdc-85f3-fa25c7f7c429
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 63187739
Hyphenated Format 63187-739

Supplemental Identifiers

RxCUI
310429
UPC
0363187739300
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 ANDA077293 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 10 TABLET in 1 BOTTLE (63187-739-10)
  • 30 TABLET in 1 BOTTLE (63187-739-30)
  • 60 TABLET in 1 BOTTLE (63187-739-60)
  • 90 TABLET in 1 BOTTLE (63187-739-90)
source: ndc

Packages (4)

63187-739-10 10 TABLET in 1 BOTTLE (63187-739-10) 63187-739-30 30 TABLET in 1 BOTTLE (63187-739-30) 63187-739-60 60 TABLET in 1 BOTTLE (63187-739-60) 63187-739-90 90 TABLET in 1 BOTTLE (63187-739-90)

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": "7a15b0c4-de78-4bdc-85f3-fa25c7f7c429", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0363187739300"], "unii": ["7LXU5N7ZO5"], "rxcui": ["310429"], "spl_set_id": ["595ddaf2-c2cb-44a4-a46c-53bcfe6bd752"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE (63187-739-10)", "package_ndc": "63187-739-10", "marketing_start_date": "20170301"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (63187-739-30)", "package_ndc": "63187-739-30", "marketing_start_date": "20161003"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (63187-739-60)", "package_ndc": "63187-739-60", "marketing_start_date": "20161003"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (63187-739-90)", "package_ndc": "63187-739-90", "marketing_start_date": "20161003"}], "brand_name": "Furosemide", "product_id": "63187-739_7a15b0c4-de78-4bdc-85f3-fa25c7f7c429", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "63187-739", "generic_name": "Furosemide", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "20 mg/1"}], "application_number": "ANDA077293", "marketing_category": "ANDA", "marketing_start_date": "20060201", "listing_expiration_date": "20261231"}