furosemide

Generic: furosemide

Labeler: solco healthcare llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

furosemide 80 mg/1

Manufacturer
Solco Healthcare LLC

Identifiers & Regulatory

Product NDC 43547-403
Product ID 43547-403_800a897c-46f4-4983-b07e-697ef21afb46
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076796
Listing Expiration 2026-12-31
Marketing Start 2004-03-26

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 43547403
Hyphenated Format 43547-403

Supplemental Identifiers

RxCUI
197732 310429 313988
UPC
0343547402105 0343547403102 0343547401108
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 ANDA076796 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 80 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (43547-403-10)
  • 1000 TABLET in 1 BOTTLE, PLASTIC (43547-403-11)
  • 500 TABLET in 1 BOTTLE, PLASTIC (43547-403-50)
  • 500000 TABLET in 1 DRUM (43547-403-94)
source: ndc

Packages (4)

43547-403-10 100 TABLET in 1 BOTTLE, PLASTIC (43547-403-10) 43547-403-11 1000 TABLET in 1 BOTTLE, PLASTIC (43547-403-11) 43547-403-50 500 TABLET in 1 BOTTLE, PLASTIC (43547-403-50) 43547-403-94 500000 TABLET in 1 DRUM (43547-403-94)

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": "800a897c-46f4-4983-b07e-697ef21afb46", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0343547402105", "0343547403102", "0343547401108"], "unii": ["7LXU5N7ZO5"], "rxcui": ["197732", "310429", "313988"], "spl_set_id": ["6a0fb397-63ae-4fce-bddf-16a91b1b7a2f"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Solco Healthcare LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (43547-403-10)", "package_ndc": "43547-403-10", "marketing_start_date": "20040326"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (43547-403-11)", "package_ndc": "43547-403-11", "marketing_start_date": "20040326"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (43547-403-50)", "package_ndc": "43547-403-50", "marketing_start_date": "20040326"}, {"sample": false, "description": "500000 TABLET in 1 DRUM (43547-403-94)", "package_ndc": "43547-403-94", "marketing_start_date": "20220101"}], "brand_name": "Furosemide", "product_id": "43547-403_800a897c-46f4-4983-b07e-697ef21afb46", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "43547-403", "generic_name": "furosemide", "labeler_name": "Solco Healthcare LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "80 mg/1"}], "application_number": "ANDA076796", "marketing_category": "ANDA", "marketing_start_date": "20040326", "listing_expiration_date": "20261231"}