NDC 43353-747

Furosemide

Furosemide

Furosemide is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Aphena Pharma Solutions - Tennessee, Llc. The primary component is Furosemide.

Product ID43353-747_13d5f0a8-f822-4190-99b3-32f2a1126caf
NDC43353-747
Product TypeHuman Prescription Drug
Proprietary NameFurosemide
Generic NameFurosemide
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date1983-11-10
Marketing CategoryNDA / NDA
Application NumberNDA018823
Labeler NameAphena Pharma Solutions - Tennessee, LLC
Substance NameFUROSEMIDE
Active Ingredient Strength20 mg/1
Pharm ClassesIncreased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 43353-747-30

30 TABLET in 1 BOTTLE, PLASTIC (43353-747-30)
Marketing Start Date2017-05-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 43353-747-92 [43353074792]

Furosemide TABLET
Marketing CategoryNDA
Application NumberNDA018823
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-08-22

NDC 43353-747-60 [43353074760]

Furosemide TABLET
Marketing CategoryNDA
Application NumberNDA018823
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2011-08-02

NDC 43353-747-53 [43353074753]

Furosemide TABLET
Marketing CategoryNDA
Application NumberNDA018823
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-05-01

NDC 43353-747-30 [43353074730]

Furosemide TABLET
Marketing CategoryNDA
Application NumberNDA018823
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-05-01

NDC 43353-747-80 [43353074780]

Furosemide TABLET
Marketing CategoryNDA
Application NumberNDA018823
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-05-01

NDC 43353-747-45 [43353074745]

Furosemide TABLET
Marketing CategoryNDA
Application NumberNDA018823
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-08-22

Drug Details

Active Ingredients

IngredientStrength
FUROSEMIDE20 mg/1

OpenFDA Data

SPL SET ID:6fbf7f3d-7566-44d5-9507-c4460238fc91
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 310429
  • 313988
  • Pharmacological Class

    • Increased Diuresis at Loop of Henle [PE]
    • Loop Diuretic [EPC]
    • Increased Diuresis at Loop of Henle [PE]
    • Loop Diuretic [EPC]

    NDC Crossover Matching brand name "Furosemide" or generic name "Furosemide"

    NDCBrand NameGeneric Name
    0054-3294FurosemideFurosemide
    0054-3298FurosemideFurosemide
    0054-4297FurosemideFurosemide
    0054-4299FurosemideFurosemide
    0054-4301FurosemideFurosemide
    0054-8297FurosemideFurosemide
    0054-8299FurosemideFurosemide
    0054-8301FurosemideFurosemide
    0378-0208Furosemidefurosemide
    0378-0216Furosemidefurosemide
    0378-0232Furosemidefurosemide
    0404-9861FurosemideFurosemide
    0404-9862FUROSEMIDEfurosemide
    0404-9863FurosemideFurosemide
    0404-9864FUROSEMIDEfurosemide
    0409-1639FurosemideFUROSEMIDE
    0409-6102FUROSEMIDEFUROSEMIDE
    68071-1708FurosemideFurosemide
    68071-1809FurosemideFurosemide
    68071-3273FurosemideFurosemide
    68071-3144FurosemideFurosemide
    68071-3194FurosemideFurosemide
    68071-3148FurosemideFurosemide
    68071-4015FurosemideFurosemide
    68071-4022FurosemideFurosemide
    68071-4349FurosemideFurosemide
    68071-4534FurosemideFurosemide
    0409-9631FurosemideFurosemide
    68071-4445FurosemideFurosemide
    68071-4522FurosemideFurosemide
    68094-867FurosemideFurosemide
    68094-756FurosemideFurosemide
    68788-1966FurosemideFurosemide
    68788-6397FurosemideFurosemide
    68788-6784FurosemideFurosemide
    68788-7265FurosemideFurosemide
    68788-6948FurosemideFurosemide
    68788-9226FurosemideFurosemide
    68788-7354FurosemideFurosemide
    68788-9778FurosemideFurosemide
    69315-116FurosemideFurosemide
    69315-118FurosemideFurosemide
    69315-117FurosemideFurosemide
    69677-204FurosemideFurosemide
    70121-1164FurosemideFurosemide
    70121-1076FurosemideFurosemide
    70121-1163FurosemideFurosemide
    70518-0092FurosemideFurosemide
    70518-0584FurosemideFurosemide
    70518-0120FurosemideFurosemide

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