NDC 68071-3023

Bumetanide

Bumetanide

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

Product ID68071-3023_4ab651d4-61b1-51c3-e054-00144ff8d46c
NDC68071-3023
Product TypeHuman Prescription Drug
Proprietary NameBumetanide
Generic NameBumetanide
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date1996-11-21
Marketing CategoryANDA / ANDA
Application NumberANDA074700
Labeler NameNuCare Pharmaceuticals, Inc..
Substance NameBUMETANIDE
Active Ingredient Strength2 mg/1
Pharm ClassesLoop Diuretic [EPC],Increased Diuresis at Loop of Henle [PE]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 68071-3023-9

90 TABLET in 1 BOTTLE (68071-3023-9)
Marketing Start Date2017-03-14
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68071-3023-9 [68071302309]

Bumetanide TABLET
Marketing CategoryANDA
Application NumberANDA074700
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-03-14
Marketing End Date2020-12-31

NDC 68071-3023-3 [68071302303]

Bumetanide TABLET
Marketing CategoryANDA
Application NumberANDA074700
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-03-14
Marketing End Date2020-12-31

NDC 68071-3023-6 [68071302306]

Bumetanide TABLET
Marketing CategoryANDA
Application NumberANDA074700
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-03-14
Marketing End Date2020-12-31

Drug Details

Active Ingredients

IngredientStrength
BUMETANIDE2 mg/1

OpenFDA Data

SPL SET ID:4ab651d4-61b0-51c3-e054-00144ff8d46c
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 197419

    • Pharmacological Class

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