furosemide

Generic: furosemide

Labeler: phlow corporation
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name furosemide
Generic Name furosemide
Labeler phlow corporation
Dosage Form INJECTION, SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

furosemide 10 mg/mL

Manufacturer
Phlow Corporation

Identifiers & Regulatory

Product NDC 81565-201
Product ID 81565-201_e70f323d-2e94-4824-bb92-d43013caa497
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA018902
Listing Expiration 2027-12-31
Marketing Start 2022-02-01

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 81565201
Hyphenated Format 81565-201

Supplemental Identifiers

RxCUI
1719290
UPC
0381565201010
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 NDA018902 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 10 mg/mL
source: ndc
Packaging
  • 25 VIAL in 1 TRAY (81565-201-02) / 2 mL in 1 VIAL (81565-201-01)
source: ndc

Packages (1)

81565-201-02 25 VIAL in 1 TRAY (81565-201-02) / 2 mL in 1 VIAL (81565-201-01)

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": "e70f323d-2e94-4824-bb92-d43013caa497", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0381565201010"], "unii": ["7LXU5N7ZO5"], "rxcui": ["1719290"], "spl_set_id": ["08a44bdd-028d-41af-9d4e-70971b0bcc4e"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Phlow Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 TRAY (81565-201-02)  / 2 mL in 1 VIAL (81565-201-01)", "package_ndc": "81565-201-02", "marketing_start_date": "20220201"}], "brand_name": "Furosemide", "product_id": "81565-201_e70f323d-2e94-4824-bb92-d43013caa497", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "81565-201", "generic_name": "FUROSEMIDE", "labeler_name": "Phlow Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "10 mg/mL"}], "application_number": "NDA018902", "marketing_category": "NDA", "marketing_start_date": "20220201", "listing_expiration_date": "20271231"}