lasix

Generic: furosemide

Labeler: validus pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name lasix
Generic Name furosemide
Labeler validus pharmaceuticals llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

furosemide 20 mg/1

Manufacturer
Validus Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 30698-067
Product ID 30698-067_4002943d-0b4b-4ff0-e063-6394a90ae63b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA016273
Listing Expiration 2026-12-31
Marketing Start 1978-04-24

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 30698067
Hyphenated Format 30698-067

Supplemental Identifiers

RxCUI
197732 200801 200809 205732 310429 313988
UPC
0330698060018 0330698066058 0330698067017
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 lasix (source: ndc)
Generic Name furosemide (source: ndc)
Application Number NDA016273 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (30698-067-01)
  • 1000 TABLET in 1 BOTTLE (30698-067-10)
source: ndc

Packages (2)

30698-067-01 100 TABLET in 1 BOTTLE (30698-067-01) 30698-067-10 1000 TABLET in 1 BOTTLE (30698-067-10)

Ingredients (1)

furosemide (20 mg/1)

Linked Drug Pages (1)

Lasix ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4002943d-0b4b-4ff0-e063-6394a90ae63b", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0330698060018", "0330698066058", "0330698067017"], "unii": ["7LXU5N7ZO5"], "rxcui": ["197732", "200801", "200809", "205732", "310429", "313988"], "spl_set_id": ["2c9b4d8f-0770-482d-a9e6-9c616a440b1a"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Validus Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (30698-067-01)", "package_ndc": "30698-067-01", "marketing_start_date": "19780424"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (30698-067-10)", "package_ndc": "30698-067-10", "marketing_start_date": "19780424"}], "brand_name": "Lasix", "product_id": "30698-067_4002943d-0b4b-4ff0-e063-6394a90ae63b", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "30698-067", "generic_name": "FUROSEMIDE", "labeler_name": "Validus Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lasix", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "20 mg/1"}], "application_number": "NDA016273", "marketing_category": "NDA", "marketing_start_date": "19780424", "listing_expiration_date": "20261231"}