furosemide

Generic: furosemide

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name furosemide
Generic Name furosemide
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

furosemide 20 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-6219
Product ID 50090-6219_53f4477e-13d8-402e-aa02-8a1e9addd00a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA018823
Listing Expiration 2026-12-31
Marketing Start 1983-11-10

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 500906219
Hyphenated Format 50090-6219

Supplemental Identifiers

RxCUI
310429
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 NDA018823 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (50090-6219-0)
  • 100 TABLET in 1 BOTTLE (50090-6219-1)
  • 200 TABLET in 1 BOTTLE (50090-6219-7)
  • 90 TABLET in 1 BOTTLE (50090-6219-8)
source: ndc

Packages (4)

50090-6219-0 30 TABLET in 1 BOTTLE (50090-6219-0) 50090-6219-1 100 TABLET in 1 BOTTLE (50090-6219-1) 50090-6219-7 200 TABLET in 1 BOTTLE (50090-6219-7) 50090-6219-8 90 TABLET in 1 BOTTLE (50090-6219-8)

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": "53f4477e-13d8-402e-aa02-8a1e9addd00a", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["310429"], "spl_set_id": ["a2e46e16-4adf-4599-b69d-a6f6f891ba75"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-6219-0)", "package_ndc": "50090-6219-0", "marketing_start_date": "20221110"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (50090-6219-1)", "package_ndc": "50090-6219-1", "marketing_start_date": "20221110"}, {"sample": false, "description": "200 TABLET in 1 BOTTLE (50090-6219-7)", "package_ndc": "50090-6219-7", "marketing_start_date": "20221110"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-6219-8)", "package_ndc": "50090-6219-8", "marketing_start_date": "20221110"}], "brand_name": "Furosemide", "product_id": "50090-6219_53f4477e-13d8-402e-aa02-8a1e9addd00a", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "50090-6219", "generic_name": "Furosemide", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "20 mg/1"}], "application_number": "NDA018823", "marketing_category": "NDA", "marketing_start_date": "19831110", "listing_expiration_date": "20261231"}