Furosemide

Product NDC
10544-584
11-digit product format
105440584
Labeler code
10544
Product ID
10544-584_c47fbc0b-c7c7-4002-8e0e-bb5b25be363e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Furosemide
Dosage form
TABLET
Route
ORAL
Labeler
Blenheim Pharmacal, Inc.
Application
ANDA078010
Marketing category
ANDA
Marketing start
2013-12-20
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
E
Listing certified through
2017-12-31
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
10544-584-302019-11-27C16284748780-19855e2a2-341a-60a7-e053-dbdaa90a05bdFurosemide Tablets, USP Rx Only
10544-584-902019-11-27C16284748780-19855e2a2-341a-60a7-e053-dbdaa90a05bdFurosemide Tablets, USP Rx Only

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10544-584-30Furosemide30 in 1 BOTTLETABLET301
10544-584-90Furosemide90 in 1 BOTTLETABLET901

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
10544-584-30EA - Each10544-58415147ca0-0e9f-4bac-9093-860471660fb012015-05-05
10544-584-90EA - Each10544-584362813bc-3324-48e1-823f-1b8daba6ce1412015-05-05

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
FUROSEMIDEACTIVE INGREDIENT7LXU5N7ZO5FUROSEMIDE TABLET [BLENHEIM PHARMACAL, INC.]1
FUROSEMIDEACTIVE MOIETY7LXU5N7ZO5FUROSEMIDE TABLET [BLENHEIM PHARMACAL, INC.]1
LACTOSE MONOHYDRATEINACTIVE INGREDIENTEWQ57Q8I5XFUROSEMIDE TABLET [BLENHEIM PHARMACAL, INC.]1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30FUROSEMIDE TABLET [BLENHEIM PHARMACAL, INC.]1
SODIUM STARCH GLYCOLATE TYPE A POTATOINACTIVE INGREDIENT5856J3G2A2FUROSEMIDE TABLET [BLENHEIM PHARMACAL, INC.]1
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJFUROSEMIDE TABLET [BLENHEIM PHARMACAL, INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RFUROSEMIDE TABLET [BLENHEIM PHARMACAL, INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10544-584FUROSEMIDE TABLET [BLENHEIM PHARMACAL, INC.]1Legacy NDC, 2 package rows20140205_c47fbc0b-c7c7-4002-8e0e-bb5b25be363e.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
310429furosemide 20 MG Oral TabletPSNc47fbc0b-c7c7-4002-8e0e-bb5b25be363e1
313988furosemide 40 MG Oral TabletPSNc47fbc0b-c7c7-4002-8e0e-bb5b25be363e1
310429furosemide 20 MG Oral TabletSCDc47fbc0b-c7c7-4002-8e0e-bb5b25be363e1
313988furosemide 40 MG Oral TabletSCDc47fbc0b-c7c7-4002-8e0e-bb5b25be363e1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
10544-584-301054405843030 in 1 BOTTLEHistorical
10544-584-901054405849090 in 1 BOTTLEHistorical