FDA.reportPublic FDA data

Furosemide

Product NDC
43063-702
11-digit product format
430630702
Labeler code
43063
Product ID
43063-702_4147a2fb-f8a4-1776-e063-6394a90a5185
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Furosemide
Dosage form
TABLET
Route
ORAL
Labeler
PD-Rx Pharmaceuticals, Inc.
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
43063-702-21Furosemide21 in 1 BOTTLE, PLASTICTABLET2118
43063-702-30Furosemide30 in 1 BOTTLE, PLASTICTABLET3018
43063-702-60Furosemide60 in 1 BOTTLE, PLASTICTABLET6018
43063-702-79Furosemide1 in 1 BOTTLE, PLASTICTABLET118
43063-702-90Furosemide90 in 1 BOTTLE, PLASTICTABLET9018

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
43063-702-21EA - Each43063-7021b17fc3a-031f-46b1-bb2b-cc03647f59bc12017-03-06
43063-702-30EA - Each43063-7025edfce8e-d667-431b-8db6-6265ef53e8fc12016-11-08
43063-702-60EA - Each43063-702517d6c5a-a99e-49f6-affe-e6f37937b6ca12016-09-02
43063-702-79EA - Each43063-7022ff3c42d-0633-4674-b7b6-399fbfd7582e12017-04-05
43063-702-90EA - Each43063-7029bea256c-99d0-4c7e-8416-f0ebb3feab7712017-03-06

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43063-702FUROSEMIDE (FUROSEMIDE) TABLET [PD-RX PHARMACEUTICALS, INC.]17Current NDC, Legacy NDC, 5 package rows20240906_7842eeab-decf-47e7-9134-0add90549a3d.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
310429furosemide 20 MG Oral TabletPSN7842eeab-decf-47e7-9134-0add90549a3d18
310429furosemide 20 MG Oral TabletSCD7842eeab-decf-47e7-9134-0add90549a3d18

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
43063-702-214306307022121 TABLET in 1 BOTTLE, PLASTIC (43063-702-21) 21 tablet2017-01-310000-00-00NoNoCurrent
43063-702-304306307023030 TABLET in 1 BOTTLE, PLASTIC (43063-702-30) 30 tablet2016-09-290000-00-00NoNoCurrent
43063-702-604306307026060 TABLET in 1 BOTTLE, PLASTIC (43063-702-60) 60 tablet2016-08-100000-00-00NoNoCurrent
43063-702-79430630702791 TABLET in 1 BOTTLE, PLASTIC (43063-702-79) 1 tablet2017-02-210000-00-00NoNoCurrent
43063-702-904306307029090 TABLET in 1 BOTTLE, PLASTIC (43063-702-90) 90 tablet2017-01-040000-00-00NoNoCurrent