NDC 0615-7938

Fuosemide

Furosemide

Fuosemide is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Ncs Healthcare Of Ky, Inc Dba Vangard Labs. The primary component is Furosemide.

Product ID0615-7938_8676925e-cabd-4690-9632-afed4b1211c9
NDC0615-7938
Product TypeHuman Prescription Drug
Proprietary NameFuosemide
Generic NameFurosemide
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date1983-11-10
Marketing End Date2022-10-31
Marketing CategoryNDA / NDA
Application NumberNDA018823
Labeler NameNCS HealthCare of KY, Inc dba Vangard Labs
Substance NameFUROSEMIDE
Active Ingredient Strength40 mg/1
Pharm ClassesIncreased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]
NDC Exclude FlagN

Packaging

NDC 0615-7938-05

15 TABLET in 1 BLISTER PACK (0615-7938-05)
Marketing Start Date2016-04-04
Marketing End Date2022-09-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0615-7938-39 [00615793839]

Fuosemide TABLET
Marketing CategoryNDA
Application NumberNDA018823
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1983-11-10

NDC 0615-7938-05 [00615793805]

Fuosemide TABLET
Marketing CategoryNDA
Application NumberNDA018823
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1983-11-10

NDC 0615-7938-30 [00615793830]

Fuosemide TABLET
Marketing CategoryNDA
Application NumberNDA018823
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1983-11-10

NDC 0615-7938-28 [00615793828]

Fuosemide TABLET
Marketing CategoryNDA
Application NumberNDA018823
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-07-03

NDC 0615-7938-07 [00615793807]

Fuosemide TABLET
Marketing CategoryNDA
Application NumberNDA018823
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-07-03

NDC 0615-7938-14 [00615793814]

Fuosemide TABLET
Marketing CategoryNDA
Application NumberNDA018823
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1983-11-10

Drug Details

Active Ingredients

IngredientStrength
FUROSEMIDE40 mg/1

OpenFDA Data

SPL SET ID:aaf84f86-c9ea-4d84-8bf9-3d198cfa14c3
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 197732
  • 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 "Fuosemide" or generic name "Furosemide"

    NDCBrand NameGeneric Name
    0615-7938FuosemideFuosemide
    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

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