Furosemide

Product NDC
33261-174
11-digit product format
332610174
Labeler code
33261
Product ID
33261-174_8e5a1b85-9468-4dc3-94b8-06cda657d5b3
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Furosemide
Dosage form
TABLET
Route
ORAL
Labeler
Aidarex Pharmaceuticals LLC
Application
ANDA078010
Marketing category
ANDA
Marketing start
2009-01-29
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
33261-174-00Furosemide100 in 1 BOTTLE, PLASTICTABLET1001
33261-174-08Furosemide8 in 1 BOTTLE, PLASTICTABLET81
33261-174-14Furosemide14 in 1 BOTTLE, PLASTICTABLET141
33261-174-20Furosemide20 in 1 BOTTLE, PLASTICTABLET201
33261-174-30Furosemide30 in 1 BOTTLE, PLASTICTABLET301
33261-174-60Furosemide60 in 1 BOTTLE, PLASTICTABLET601
33261-174-90Furosemide90 in 1 BOTTLE, PLASTICTABLET901

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
33261-174-00EA - Each33261-1748764fe4e-2f82-410f-a4e3-7e26ebcb9d6d12015-10-02
33261-174-08EA - Each33261-174a67f062c-3058-434f-b39f-54941d07265012016-09-02
33261-174-14EA - Each33261-174ba48be82-7a08-48d2-a8f4-df4d37713fc612016-09-02
33261-174-20EA - Each33261-1746df6da97-3c03-422d-b759-187f125ce3c612016-09-02
33261-174-30EA - Each33261-174643cbe3c-be17-4049-b798-6237931cc1e712015-10-02
33261-174-60EA - Each33261-174bdbfb274-d52c-4710-bec5-9f1c303ae0d712015-10-02
33261-174-90EA - Each33261-174904ace06-b7bb-4528-8a0e-bbfa0a01b75b12015-10-02

DailyMed Socrata Ingredients#

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

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
33261-174FUROSEMIDE TABLET [AIDAREX PHARMACEUTICALS LLC]1Legacy NDC, 7 package rows20140110_22da65c8-759c-4b06-921b-feef9bf06178.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
310429furosemide 20 MG Oral TabletPSN22da65c8-759c-4b06-921b-feef9bf061781
313988furosemide 40 MG Oral TabletPSN22da65c8-759c-4b06-921b-feef9bf061781
310429furosemide 20 MG Oral TabletSCD22da65c8-759c-4b06-921b-feef9bf061781
313988furosemide 40 MG Oral TabletSCD22da65c8-759c-4b06-921b-feef9bf061781

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
33261-174-0033261017400100 in 1 BOTTLE, PLASTICHistorical
33261-174-08332610174088 in 1 BOTTLE, PLASTICHistorical
33261-174-143326101741414 in 1 BOTTLE, PLASTICHistorical
33261-174-203326101742020 in 1 BOTTLE, PLASTICHistorical
33261-174-303326101743030 in 1 BOTTLE, PLASTICHistorical
33261-174-603326101746060 in 1 BOTTLE, PLASTICHistorical
33261-174-903326101749090 in 1 BOTTLE, PLASTICHistorical