FDA.reportPublic FDA data

Furosemide

Product NDC
71335-0384
11-digit product format
713350384
Labeler code
71335
Product ID
71335-0384_83a9fbac-05c9-4f16-8720-4c8bd1164b28
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Furosemide
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA077293
Marketing category
ANDA
Marketing start
2006-02-01
Substance
FUROSEMIDE
Active strength
20 mg/1
Pharmacologic classes
Increased Diuresis at Loop of Henle [PE], Loop Diuretic [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Furosemide
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
FUROSEMIDE20 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii7LXU5N7ZO5
Rxcui310429

DailyMed Product Concepts#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71335-0384-1Furosemide30 in 1 BOTTLETABLET30102
71335-0384-2Furosemide90 in 1 BOTTLETABLET90102
71335-0384-3Furosemide60 in 1 BOTTLETABLET60102
71335-0384-4Furosemide100 in 1 BOTTLETABLET100102
71335-0384-5Furosemide7 in 1 BOTTLETABLET7102
71335-0384-6Furosemide28 in 1 BOTTLETABLET28102
71335-0384-7Furosemide14 in 1 BOTTLETABLET14102
71335-0384-8Furosemide10 in 1 BOTTLETABLET10102
71335-0384-9Furosemide20 in 1 BOTTLETABLET20102

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71335-0384-1EA - Each71335-0384f123e74f-74fa-4bde-a4fe-d2c1c564ab2312018-02-20
71335-0384-2EA - Each71335-03840c2a9931-e3d0-4b90-a435-fc36bbb73b7212018-02-20
71335-0384-3EA - Each71335-0384d7e00952-50b3-4f82-a38d-f96883d3c3c012018-02-20
71335-0384-4EA - Each71335-0384423f3ba2-421a-444c-b01f-8ba81d275c1412018-02-20
71335-0384-5EA - Each71335-0384be5e7401-083a-4ee1-b42e-6d260027569b12018-02-20
71335-0384-6EA - Each71335-038410a30f1b-05ba-488f-9360-d2ae4d4e4e8612018-02-20
71335-0384-7EA - Each71335-03844f0b83f6-4ba2-4017-8352-27fafc272eba12018-02-20
71335-0384-8EA - Each71335-03844fb44257-c767-4e0f-b1a6-3fb80e1dd89212018-02-20

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71335-0384FUROSEMIDE (FUROSEMIDE) TABLET [BRYANT RANCH PREPACK]102Current NDC, Legacy NDC, 9 package rows20240824_0dd28e18-2e15-45eb-9a61-a9de7bd7d64e.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
310429furosemide 20 MG Oral TabletPSN0dd28e18-2e15-45eb-9a61-a9de7bd7d64e102
310429furosemide 20 MG Oral TabletSCD0dd28e18-2e15-45eb-9a61-a9de7bd7d64e102

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-0384-17133503840130 TABLET in 1 BOTTLE (71335-0384-1) 30 tablet2022-02-090000-00-00NoNoCurrent
71335-0384-27133503840290 TABLET in 1 BOTTLE (71335-0384-2) 90 tablet2022-02-090000-00-00NoNoCurrent
71335-0384-37133503840360 TABLET in 1 BOTTLE (71335-0384-3) 60 tablet2022-02-090000-00-00NoNoCurrent
71335-0384-471335038404100 TABLET in 1 BOTTLE (71335-0384-4) 100 tablet2022-02-090000-00-00NoNoCurrent
71335-0384-5713350384057 TABLET in 1 BOTTLE (71335-0384-5) 7 tablet2022-02-090000-00-00NoNoCurrent
71335-0384-67133503840628 TABLET in 1 BOTTLE (71335-0384-6) 28 tablet2022-02-090000-00-00NoNoCurrent
71335-0384-77133503840714 TABLET in 1 BOTTLE (71335-0384-7) 14 tablet2022-02-090000-00-00NoNoCurrent
71335-0384-87133503840810 TABLET in 1 BOTTLE (71335-0384-8) 10 tablet2022-02-090000-00-00NoNoCurrent
71335-0384-97133503840920 TABLET in 1 BOTTLE (71335-0384-9) 20 tablet2022-02-090000-00-00NoNoCurrent