Furosemide

Product NDC
43353-737
11-digit product format
433530737
Labeler code
43353
Product ID
43353-737_3f914177-d57c-4f45-9cf3-4b98f8354ef8
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Furosemide
Dosage form
TABLET
Route
ORAL
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Application
NDA018569
Marketing category
NDA
Marketing start
1981-10-19
Marketing end
0000-00-00
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
2019-12-31
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#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43353-737-30Furosemide30 in 1 BOTTLE, PLASTICTABLET302
43353-737-45Furosemide45 in 1 BOTTLE, PLASTICTABLET452
43353-737-53Furosemide60 in 1 BOTTLE, PLASTICTABLET602
43353-737-60Furosemide90 in 1 BOTTLE, PLASTICTABLET902
43353-737-80Furosemide180 in 1 BOTTLE, PLASTICTABLET1802
43353-737-92Furosemide270 in 1 BOTTLE, PLASTICTABLET2702
43353-737-94Furosemide360 in 1 BOTTLE, PLASTICTABLET3602

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
43353-737-30EA - Each43353-7371adece98-29dd-4af6-9006-85f7e278c02612014-06-03
43353-737-45EA - Each43353-73795c0b68d-1f9c-447e-a7f3-a340416f1cb712014-06-03
43353-737-53EA - Each43353-737a8be8bdb-c8d4-43ac-9f61-855b8d2c255412014-06-03
43353-737-60EA - Each43353-737032fdfda-1203-48f2-8d0a-fff148e7506a12014-06-03
43353-737-80EA - Each43353-7370157c3b5-3342-40fe-ad35-06fa132fe80612014-06-03
43353-737-92EA - Each43353-7373bae76c5-b5d0-4468-bbed-6cc90c6372b612014-06-03

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
FUROSEMIDEACTIVE INGREDIENT7LXU5N7ZO5FUROSEMIDE TABLET [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC]2
FUROSEMIDEACTIVE MOIETY7LXU5N7ZO5FUROSEMIDE TABLET [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC]2
LACTOSE MONOHYDRATEINACTIVE INGREDIENTEWQ57Q8I5XFUROSEMIDE TABLET [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC]2
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30FUROSEMIDE TABLET [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC]2
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJFUROSEMIDE TABLET [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC]2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43353-737FUROSEMIDE TABLET [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC]2Legacy NDC, 7 package rows20140513_86323c14-2be8-4890-a8a8-cf44341b5db8.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
310429furosemide 20 MG Oral TabletPSN86323c14-2be8-4890-a8a8-cf44341b5db82
310429furosemide 20 MG Oral TabletSCD86323c14-2be8-4890-a8a8-cf44341b5db82

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
43353-737-304335307373030 in 1 BOTTLE, PLASTICHistorical
43353-737-454335307374545 in 1 BOTTLE, PLASTICHistorical
43353-737-534335307375360 in 1 BOTTLE, PLASTICHistorical
43353-737-604335307376090 in 1 BOTTLE, PLASTICHistorical
43353-737-8043353073780180 in 1 BOTTLE, PLASTICHistorical
43353-737-9243353073792270 in 1 BOTTLE, PLASTICHistorical
43353-737-9443353073794360 in 1 BOTTLE, PLASTICHistorical