lasix onyu

Generic: furosemide

Labeler: sq innovation, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name lasix onyu
Generic Name furosemide
Labeler sq innovation, inc.
Dosage Form INJECTION
Routes
SUBCUTANEOUS
Active Ingredients

furosemide 30 mg/mL

Manufacturer
SQ Innovation, Inc.

Identifiers & Regulatory

Product NDC 81137-001
Product ID 81137-001_a67aa830-538d-4920-ac7e-9b4418362473
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA217294
Listing Expiration 2026-12-31
Marketing Start 2025-12-01

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 81137001
Hyphenated Format 81137-001

Supplemental Identifiers

RxCUI
2725542 2725546
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 onyu (source: ndc)
Generic Name furosemide (source: ndc)
Application Number NDA217294 (source: ndc)
Routes
SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 30 mg/mL
source: ndc
Packaging
  • 1 CARTON in 1 KIT (81137-001-15) / 1 CARTRIDGE in 1 CARTON / 2.67 mL in 1 CARTRIDGE
source: ndc

Packages (1)

81137-001-15 1 CARTON in 1 KIT (81137-001-15) / 1 CARTRIDGE in 1 CARTON / 2.67 mL in 1 CARTRIDGE

Ingredients (1)

furosemide (30 mg/mL)

Linked Drug Pages (1)

LASIX ONYU ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["SUBCUTANEOUS"], "spl_id": "a67aa830-538d-4920-ac7e-9b4418362473", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["2725542", "2725546"], "spl_set_id": ["cb27654f-c7a1-4796-ab08-60a5fa16f5c0"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["SQ Innovation, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 CARTON in 1 KIT (81137-001-15)  / 1 CARTRIDGE in 1 CARTON / 2.67 mL in 1 CARTRIDGE", "package_ndc": "81137-001-15", "marketing_start_date": "20251201"}], "brand_name": "LASIX ONYU", "product_id": "81137-001_a67aa830-538d-4920-ac7e-9b4418362473", "dosage_form": "INJECTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "81137-001", "generic_name": "furosemide", "labeler_name": "SQ Innovation, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LASIX ONYU", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "30 mg/mL"}], "application_number": "NDA217294", "marketing_category": "NDA", "marketing_start_date": "20251201", "listing_expiration_date": "20261231"}