furosemide

Generic: furosemide

Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name furosemide
Generic Name furosemide
Labeler heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

furosemide 10 mg/mL

Manufacturer
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 23155-473
Product ID 23155-473_936eaafa-5088-4ebc-85bc-685ffb85c81f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203428
Listing Expiration 2026-12-31
Marketing Start 2014-09-02

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 23155473
Hyphenated Format 23155-473

Supplemental Identifiers

RxCUI
1719286 1719290 1719291
UPC
0323155473315 0323155473414 0323155473322 0323155473339
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 ANDA203428 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 10 mg/mL
source: ndc
Packaging
  • 25 VIAL in 1 CARTON (23155-473-41) / 2 mL in 1 VIAL (23155-473-31)
  • 25 VIAL in 1 CARTON (23155-473-42) / 4 mL in 1 VIAL (23155-473-32)
  • 50 VIAL in 1 CARTON (23155-473-43) / 4 mL in 1 VIAL (23155-473-32)
  • 25 VIAL in 1 CARTON (23155-473-44) / 10 mL in 1 VIAL (23155-473-33)
  • 50 VIAL in 1 CARTON (23155-473-45) / 10 mL in 1 VIAL (23155-473-33)
source: ndc

Packages (5)

23155-473-41 25 VIAL in 1 CARTON (23155-473-41) / 2 mL in 1 VIAL (23155-473-31) 23155-473-42 25 VIAL in 1 CARTON (23155-473-42) / 4 mL in 1 VIAL (23155-473-32) 23155-473-43 50 VIAL in 1 CARTON (23155-473-43) / 4 mL in 1 VIAL (23155-473-32) 23155-473-44 25 VIAL in 1 CARTON (23155-473-44) / 10 mL in 1 VIAL (23155-473-33) 23155-473-45 50 VIAL in 1 CARTON (23155-473-45) / 10 mL in 1 VIAL (23155-473-33)

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": ["INTRAVENOUS"], "spl_id": "936eaafa-5088-4ebc-85bc-685ffb85c81f", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0323155473315", "0323155473414", "0323155473322", "0323155473339"], "unii": ["7LXU5N7ZO5"], "rxcui": ["1719286", "1719290", "1719291"], "spl_set_id": ["1b9117d5-0dd9-4577-a1fd-bb0aaf7e68ec"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (23155-473-41)  / 2 mL in 1 VIAL (23155-473-31)", "package_ndc": "23155-473-41", "marketing_start_date": "20140902"}, {"sample": false, "description": "25 VIAL in 1 CARTON (23155-473-42)  / 4 mL in 1 VIAL (23155-473-32)", "package_ndc": "23155-473-42", "marketing_start_date": "20140902"}, {"sample": false, "description": "50 VIAL in 1 CARTON (23155-473-43)  / 4 mL in 1 VIAL (23155-473-32)", "package_ndc": "23155-473-43", "marketing_start_date": "20140902"}, {"sample": false, "description": "25 VIAL in 1 CARTON (23155-473-44)  / 10 mL in 1 VIAL (23155-473-33)", "package_ndc": "23155-473-44", "marketing_start_date": "20140902"}, {"sample": false, "description": "50 VIAL in 1 CARTON (23155-473-45)  / 10 mL in 1 VIAL (23155-473-33)", "package_ndc": "23155-473-45", "marketing_start_date": "20140902"}], "brand_name": "Furosemide", "product_id": "23155-473_936eaafa-5088-4ebc-85bc-685ffb85c81f", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "23155-473", "generic_name": "Furosemide", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "10 mg/mL"}], "application_number": "ANDA203428", "marketing_category": "ANDA", "marketing_start_date": "20140902", "listing_expiration_date": "20261231"}