furosemide

Generic: furosemide

Labeler: hf acquisition co llc, dba healthfirst
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name furosemide
Generic Name furosemide
Labeler hf acquisition co llc, dba healthfirst
Dosage Form INJECTION, SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

furosemide 10 mg/mL

Manufacturer
HF Acquisition Co LLC, DBA HealthFirst

Identifiers & Regulatory

Product NDC 51662-1226
Product ID 51662-1226_0f8e7f56-23e5-8931-e063-6294a90af687
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA018667
Listing Expiration 2026-12-31
Marketing Start 2018-09-14

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 516621226
Hyphenated Format 51662-1226

Supplemental Identifiers

RxCUI
1719286
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 NDA018667 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 10 mg/mL
source: ndc
Packaging
  • 10 mL in 1 VIAL, SINGLE-USE (51662-1226-1)
  • 25 POUCH in 1 CASE (51662-1226-3) / 1 VIAL, SINGLE-USE in 1 POUCH (51662-1226-2) / 10 mL in 1 VIAL, SINGLE-USE
source: ndc

Packages (2)

51662-1226-1 10 mL in 1 VIAL, SINGLE-USE (51662-1226-1) 51662-1226-3 25 POUCH in 1 CASE (51662-1226-3) / 1 VIAL, SINGLE-USE in 1 POUCH (51662-1226-2) / 10 mL in 1 VIAL, SINGLE-USE

Ingredients (1)

furosemide (10 mg/mL)

Linked Drug Pages (1)

FUROSEMIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "0f8e7f56-23e5-8931-e063-6294a90af687", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["1719286"], "spl_set_id": ["75d5611a-f9e0-1841-e053-2991aa0af415"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "10 mL in 1 VIAL, SINGLE-USE (51662-1226-1)", "package_ndc": "51662-1226-1", "marketing_start_date": "20180914"}, {"sample": false, "description": "25 POUCH in 1 CASE (51662-1226-3)  / 1 VIAL, SINGLE-USE in 1 POUCH (51662-1226-2)  / 10 mL in 1 VIAL, SINGLE-USE", "package_ndc": "51662-1226-3", "marketing_start_date": "20220422"}], "brand_name": "FUROSEMIDE", "product_id": "51662-1226_0f8e7f56-23e5-8931-e063-6294a90af687", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "51662-1226", "generic_name": "FUROSEMIDE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FUROSEMIDE", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "10 mg/mL"}], "application_number": "NDA018667", "marketing_category": "NDA", "marketing_start_date": "20180914", "listing_expiration_date": "20261231"}