NDC 43353-018

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 ID43353-018_6b8291f1-dcbd-4c61-92a4-9b1d35eeecdc
NDC43353-018
Product TypeHuman Prescription Drug
Proprietary NameFurosemide
Generic NameFurosemide
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2006-02-01
Marketing CategoryANDA / ANDA
Application NumberANDA077293
Labeler NameAphena Pharma Solutions - Tennessee, LLC
Substance NameFUROSEMIDE
Active Ingredient Strength40 mg/1
Pharm ClassesIncreased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 43353-018-30

30 TABLET in 1 BOTTLE (43353-018-30)
Marketing Start Date2015-04-07
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 43353-018-60 [43353001860]

Furosemide TABLET
Marketing CategoryANDA
Application NumberANDA077293
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2015-04-07

NDC 43353-018-53 [43353001853]

Furosemide TABLET
Marketing CategoryANDA
Application NumberANDA077293
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2015-04-07

NDC 43353-018-80 [43353001880]

Furosemide TABLET
Marketing CategoryANDA
Application NumberANDA077293
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2015-04-07

NDC 43353-018-30 [43353001830]

Furosemide TABLET
Marketing CategoryANDA
Application NumberANDA077293
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2015-04-07

NDC 43353-018-45 [43353001845]

Furosemide TABLET
Marketing CategoryANDA
Application NumberANDA077293
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2015-04-07

Drug Details

Active Ingredients

IngredientStrength
FUROSEMIDE40 mg/1

OpenFDA Data

SPL SET ID:f7aec34c-2373-483c-b89c-2c53320f3829
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 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

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.