FDA.reportPublic FDA data

NDC 58829-303 - Furosemide 1%

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
58829-303
Package NDCs from labels
58829-303-60
Manufacturer
FIRST PRIORITY INCORPORATED
Effective date
2023-11-02
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Furosemide 1% - FIRST PRIORITY INCORPORATEDFIRST PRIORITY INCORPORATED2023-11-02PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58829-303-60Furosemide1%12 in 1 CASESYRUP126
58829-303-60Furosemide1%1 in 1 CARTONSYRUP16

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58829-303FUROSEMIDE 1% (FUROSEMIDE) SYRUP [FIRST PRIORITY INCORPORATED]62 package rows20231103_9ca6640e-dbfb-4bcd-bf3e-c8c68b7d41a1.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
FUROSEMIDEACTIVE INGREDIENT7LXU5N7ZO5FUROSEMIDE 1% (FUROSEMIDE) SYRUP [FIRST PRIORITY INCORPORATED]3
FUROSEMIDEACTIVE MOIETY7LXU5N7ZO5FUROSEMIDE 1% (FUROSEMIDE) SYRUP [FIRST PRIORITY INCORPORATED]3

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 8 of 8 · 148 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
FurosemideFUROSEMIDELeading Pharma, LLCb5c6fcf4-fd37-4fee-8dac-1a3273d95ffe2022-11-11Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEPrecision Dose Inc.4a746634-379b-4847-a965-7607d2a71bed2022-09-21Warnings, Adverse reactionsExact identifier
rxcui: 197730
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEAphena Pharma Solutions - Tennessee, LLC6f124d7d-a19d-4de6-8ea4-719a42eb520b2022-03-10Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FUROSEMIDEFUROSEMIDEHF Acquisition Co LLC, DBA HealthFirstc5d9b063-e3fe-ec2f-e053-2995a90ab3f22021-06-28Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEProficient Rx LPce84359c-2f76-421a-9b2b-79b1c2be2f202021-01-01Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEGland Pharma Limited644704c0-e6a5-4804-bfa6-795c8f83aa7a2020-07-03Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEAphena Pharma Solutions - Tennessee, LLC1d2733ac-6fa6-44d1-96d4-f1a698045ad22018-04-18Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEAphena Pharma Solutions - Tennessee, LLC6fbf7f3d-7566-44d5-9507-c4460238fc912018-02-09Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5

Reported adverse events (FAERS/openFDA)#

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