FDA.reportPublic FDA data

Furosemide

Product NDC
71610-308
11-digit product format
716100308
Labeler code
71610
Product ID
71610-308_f0960a17-009b-4da4-b2cc-7851e22a2165
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Furosemide
Dosage form
TABLET
Route
ORAL
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Application
NDA018823
Marketing category
NDA
Marketing start
1983-11-10
Marketing end
0000-00-00
Substance
FUROSEMIDE
Active strength
40 mg/1
Pharmacologic classes
Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d80d3aff-3a63-4d7b-a2be-fd9388b04330Product name920250806
9061e89f-9c86-4196-b34b-886fc1673cc4Product name120140821

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71610-308-302023-01-30C16284748780-1f386c649-b912-0266-e053-dadaa90a7c1aFUROSEMIDE Tablets USP
71610-308-452023-01-30C16284748780-1f386c649-b912-0266-e053-dadaa90a7c1aFUROSEMIDE Tablets USP
71610-308-532023-01-30C16284748780-1f386c649-b912-0266-e053-dadaa90a7c1aFUROSEMIDE Tablets USP
71610-308-602023-01-30C16284748780-1f386c649-b912-0266-e053-dadaa90a7c1aFUROSEMIDE Tablets USP
71610-308-802023-01-30C16284748780-1f386c649-b912-0266-e053-dadaa90a7c1aFUROSEMIDE Tablets USP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71610-308-30Furosemide30 in 1 BOTTLETABLET301
71610-308-45Furosemide45 in 1 BOTTLETABLET451
71610-308-53Furosemide60 in 1 BOTTLETABLET601
71610-308-60Furosemide90 in 1 BOTTLETABLET901
71610-308-80Furosemide180 in 1 BOTTLETABLET1801

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71610-308-30EA - Each71610-308906b4b45-5f32-4b47-9c74-6c57f2e92ef512019-09-05
71610-308-45EA - Each71610-3085e15d534-df5e-4d7f-adbb-14aea35477c512019-10-07
71610-308-53EA - Each71610-308d026aac3-1b42-4404-b4ae-d66c3a13938612019-09-05
71610-308-60EA - Each71610-308b02bb1ac-cc39-4233-8a77-dc6db5fad68a12019-09-05
71610-308-80EA - Each71610-30828246d4c-092d-4036-bcf1-622a1293d30012019-09-05

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71610-308FUROSEMIDE TABLET [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC]1Legacy NDC, 5 package rows20190817_a0dd45a3-4ae8-4301-8d6c-a20eac80cb2c.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
310429furosemide 20 MG Oral TabletPSNa0dd45a3-4ae8-4301-8d6c-a20eac80cb2c1
313988furosemide 40 MG Oral TabletPSNa0dd45a3-4ae8-4301-8d6c-a20eac80cb2c1
197732furosemide 80 MG Oral TabletPSNa0dd45a3-4ae8-4301-8d6c-a20eac80cb2c1
310429furosemide 20 MG Oral TabletSCDa0dd45a3-4ae8-4301-8d6c-a20eac80cb2c1
313988furosemide 40 MG Oral TabletSCDa0dd45a3-4ae8-4301-8d6c-a20eac80cb2c1
197732furosemide 80 MG Oral TabletSCDa0dd45a3-4ae8-4301-8d6c-a20eac80cb2c1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71610-308-307161003083030 TABLET in 1 BOTTLE (71610-308-30) 30 tablet2019-07-160000-00-00NoNoCurrent
71610-308-457161003084545 TABLET in 1 BOTTLE (71610-308-45) 45 tablet2019-07-160000-00-00NoNoCurrent
71610-308-537161003085360 TABLET in 1 BOTTLE (71610-308-53) 60 tablet2019-07-170000-00-00NoNoCurrent
71610-308-607161003086090 TABLET in 1 BOTTLE (71610-308-60) 90 tablet2019-07-160000-00-00NoNoCurrent
71610-308-8071610030880180 TABLET in 1 BOTTLE (71610-308-80) 180 tablet2019-07-160000-00-00NoNoCurrent