NDC 0185-0130

Bumetanide

Bumetanide

Bumetanide is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Eon Labs, Inc.. The primary component is Bumetanide.

Product ID0185-0130_0541dab4-9ca2-4c8f-b70a-42f64547b808
NDC0185-0130
Product TypeHuman Prescription Drug
Proprietary NameBumetanide
Generic NameBumetanide
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date1996-11-21
Marketing CategoryANDA / ANDA
Application NumberANDA074700
Labeler NameEon Labs, Inc.
Substance NameBUMETANIDE
Active Ingredient Strength2 mg/1
Pharm ClassesIncreased Diuresis at Loop of Henle [PE], Loop Diuretic [EPC]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 0185-0130-01

100 TABLET in 1 BOTTLE (0185-0130-01)
Marketing Start Date1996-11-21
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0185-0130-01 [00185013001]

Bumetanide TABLET
Marketing CategoryANDA
Application NumberANDA074700
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1996-11-21

NDC 0185-0130-05 [00185013005]

Bumetanide TABLET
Marketing CategoryANDA
Application NumberANDA074700
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1996-11-21

Drug Details

Active Ingredients

IngredientStrength
BUMETANIDE2 mg/1

OpenFDA Data

SPL SET ID:05cb961d-ac33-4bcf-b04e-411e496c43c1
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 197418
  • 197419
  • 197417
  • UPC Code
  • 0301850130016
  • Pharmacological Class

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

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

    NDCBrand NameGeneric Name
    0185-0128BumetanideBumetanide
    0185-0129BumetanideBumetanide
    0185-0130BumetanideBumetanide
    0409-1412BumetanideBUMETANIDE
    0615-4536BumetanideBumetanide
    0615-5534BumetanideBumetanide
    0615-8361bumetanidebumetanide
    0615-8362bumetanidebumetanide
    0615-8393BumetanideBumetanide
    0615-8394BumetanideBumetanide
    0641-6007BumetanideBumetanide
    0641-6008BumetanideBumetanide
    0641-6161BumetanideBumetanide
    0641-6162BumetanideBumetanide
    0832-0540BumetanideBUMETANIDE
    0832-0541BumetanideBUMETANIDE
    0832-0542BumetanideBUMETANIDE
    0904-7016BumetanideBumetanide
    14539-700bumetanidebumetanide
    14539-701bumetanidebumetanide
    14539-702bumetanidebumetanide
    16714-831bumetanidebumetanide
    16714-832bumetanidebumetanide
    16714-833bumetanidebumetanide
    68071-3023BumetanideBumetanide
    68071-2019BumetanideBumetanide
    68071-3128BumetanideBumetanide
    68071-4350BumetanideBumetanide
    68071-4330BumetanideBumetanide
    68151-1744BumetanideBumetanide
    68151-0087BumetanideBumetanide
    68382-525bumetanidebumetanide
    68382-527bumetanidebumetanide
    68382-526bumetanidebumetanide
    69238-1489BumetanideBumetanide
    69238-1491BumetanideBumetanide
    69238-1490BumetanideBumetanide
    70518-1991BumetanideBumetanide
    70771-1025bumetanidebumetanide
    70771-1026bumetanidebumetanide
    70771-1024bumetanidebumetanide
    71335-0016BumetanideBumetanide
    33261-983BumetanideBumetanide
    42799-120BumetanideBumetanide
    42799-121BumetanideBumetanide
    42799-119BumetanideBumetanide
    43353-292BumetanideBumetanide
    43353-288BumetanideBumetanide
    50436-0129BumetanideBumetanide
    55154-4733BumetanideBumetanide

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