Furosemide

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Furosemide
Generic name: FUROSEMIDE
Manufacturer: Maiva Pharma Private Limited
Product type: HUMAN PRESCRIPTION DRUG
SPL set ID: e5880bf4-5037-4813-b7cc-656a6832ecb5
SPL ID: dddc74d0-e63a-431b-a222-12c45bdc0c16
Version: 1
Effective date: 2025-06-13
Source export date: 2026-09-28
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:20:38

Harmonized routes table
Harmonized routes
INTRAVENOUS

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 20 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application applno	ANDA	203428	derived:openfda.application_number
application number		ANDA203428	openfda.application_number
brand name		Furosemide	openfda.brand_name
generic name		FUROSEMIDE	openfda.generic_name
manufacturer name		Maiva Pharma Private Limited	openfda.manufacturer_name
ndc	package	73542-103-25	openfda.package_ndc
ndc	package	73542-102-25	openfda.package_ndc
ndc	package	73542-101-25	openfda.package_ndc
ndc	product	73542-103	openfda.product_ndc
ndc	product	73542-102	openfda.product_ndc
ndc	product	73542-101	openfda.product_ndc
ndc11	package	73542010325	derived:openfda.package_ndc
ndc11	package	73542010125	derived:openfda.package_ndc
ndc11	package	73542010225	derived:openfda.package_ndc
rxcui		1719290	openfda.rxcui
rxcui		1719291	openfda.rxcui
rxcui		1719286	openfda.rxcui
spl id		dddc74d0-e63a-431b-a222-12c45bdc0c16	id
spl set id		e5880bf4-5037-4813-b7cc-656a6832ecb5	set_id
unii		7LXU5N7ZO5	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS Furosemide is a potent diuretic which, if given in excessive amounts, can lead to a profound diuresis with water and electrolyte depletion. Therefore, careful medical supervision is required and dose and dose schedule must be adjusted to the individual patient's needs. (See DOSAGE AND ADMINISTRATION.)

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.