furosemide

Generic: furosemide

Labeler: calvin scott & co., inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name furosemide
Generic Name furosemide
Labeler calvin scott & co., inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

furosemide 40 mg/1

Manufacturer
Calvin Scott & Co., Inc.

Identifiers & Regulatory

Product NDC 17224-185
Product ID 17224-185_166340cd-364a-14fd-e063-6294a90a03b4
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 17224185
Hyphenated Format 17224-185

Supplemental Identifiers

RxCUI
313988
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
  • 40 mg/1
source: ndc
Packaging
  • 21 TABLET in 1 BOTTLE, PLASTIC (17224-185-21)
source: ndc

Packages (1)

17224-185-21 21 TABLET in 1 BOTTLE, PLASTIC (17224-185-21)

Ingredients (1)

furosemide (40 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": "166340cd-364a-14fd-e063-6294a90a03b4", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["313988"], "spl_set_id": ["b2cc89e5-6619-4113-ad31-48076652c856"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Calvin Scott & Co., Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET in 1 BOTTLE, PLASTIC (17224-185-21)", "package_ndc": "17224-185-21", "marketing_start_date": "20160515"}], "brand_name": "Furosemide", "product_id": "17224-185_166340cd-364a-14fd-e063-6294a90a03b4", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "17224-185", "generic_name": "FUROSEMIDE", "labeler_name": "Calvin Scott & Co., Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "40 mg/1"}], "application_number": "ANDA077293", "marketing_category": "ANDA", "marketing_start_date": "20060201", "listing_expiration_date": "20261231"}