FDA.reportPublic FDA data

FUROSEMIDE

Product NDC
61919-242
11-digit product format
619190242
Labeler code
61919
Product ID
61919-242_eac39a9f-9e73-3866-e053-2a95a90a5768
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
FUROSEMIDE
Dosage form
TABLET
Route
ORAL
Labeler
DIRECT RX
Application
ANDA077293
Marketing category
ANDA
Marketing start
2020-06-18
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
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
FUROSEMIDE
Listing expiration
2027-12-31

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
61919-242-302025-01-31C16284748780-11030e365-2e53-111a-e063-dadaa90a10e2FUROSEMIDE

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61919-242-30FUROSEMIDE30 in 1 BOTTLETABLET306
61919-242-90FUROSEMIDE90 in 1 BOTTLETABLET906

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
61919-242-30EA - Each61919-2422e7c51a4-82e8-4f81-a13e-a665c2e18a1712020-08-06
61919-242-90EA - Each61919-242bf147781-f020-4193-b4ee-47d640e8e3cf12026-03-17

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
FUROSEMIDEACTIVE INGREDIENT7LXU5N7ZO5FUROSEMIDE TABLET [DIRECT RX]1
FUROSEMIDEACTIVE MOIETY7LXU5N7ZO5FUROSEMIDE TABLET [DIRECT RX]1
LACTOSE MONOHYDRATEINACTIVE INGREDIENTEWQ57Q8I5XFUROSEMIDE TABLET [DIRECT RX]1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30FUROSEMIDE TABLET [DIRECT RX]1
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJFUROSEMIDE TABLET [DIRECT RX]1
TALCINACTIVE INGREDIENT7SEV7J4R1UFUROSEMIDE TABLET [DIRECT RX]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61919-242FUROSEMIDE TABLET [DIRECT RX]5Current NDC, Legacy NDC, 2 package rows20200626_9ec7808e-9201-4b8c-9790-d329320dc6c4.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
310429furosemide 20 MG Oral TabletPSN9ec7808e-9201-4b8c-9790-d329320dc6c46
310429furosemide 20 MG Oral TabletSCD9ec7808e-9201-4b8c-9790-d329320dc6c46

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
61919-242-306191902423030 TABLET in 1 BOTTLE (61919-242-30) 30 tablet2020-06-180000-00-00NoNoCurrent
61919-242-906191902429090 TABLET in 1 BOTTLE (61919-242-90) 90 tablet2020-06-18NoNoCurrent