furosemide

Generic: furosemide

Labeler: eugia us llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name furosemide
Generic Name furosemide
Labeler eugia us llc
Dosage Form INJECTION, SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

furosemide 40 mg/4mL

Manufacturer
Eugia US LLC

Identifiers & Regulatory

Product NDC 55150-323
Product ID 55150-323_9bb2ffa4-0891-4197-a970-90b178bbfad9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212174
Listing Expiration 2026-12-31
Marketing Start 2019-05-03

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 55150323
Hyphenated Format 55150-323

Supplemental Identifiers

RxCUI
1719286 1719290 1719291
UPC
0355150324019 0355150323012
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 ANDA212174 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 40 mg/4mL
source: ndc
Packaging
  • 25 VIAL in 1 CARTON (55150-323-25) / 4 mL in 1 VIAL (55150-323-01)
source: ndc

Packages (1)

55150-323-25 25 VIAL in 1 CARTON (55150-323-25) / 4 mL in 1 VIAL (55150-323-01)

Ingredients (1)

furosemide (40 mg/4mL)

Linked Drug Pages (1)

Furosemide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "9bb2ffa4-0891-4197-a970-90b178bbfad9", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0355150324019", "0355150323012"], "unii": ["7LXU5N7ZO5"], "rxcui": ["1719286", "1719290", "1719291"], "spl_set_id": ["421aa6d5-623b-4dc2-abd5-bb9e7765bf37"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Eugia US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (55150-323-25)  / 4 mL in 1 VIAL (55150-323-01)", "package_ndc": "55150-323-25", "marketing_start_date": "20190503"}], "brand_name": "Furosemide", "product_id": "55150-323_9bb2ffa4-0891-4197-a970-90b178bbfad9", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "55150-323", "generic_name": "Furosemide", "labeler_name": "Eugia US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "40 mg/4mL"}], "application_number": "ANDA212174", "marketing_category": "ANDA", "marketing_start_date": "20190503", "listing_expiration_date": "20261231"}