NDC 0615-4536

Bumetanide

Bumetanide

Bumetanide 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 Bumetanide.

Product ID0615-4536_21a6d2e6-8373-4f3f-8274-84e888b1dd6d
NDC0615-4536
Product TypeHuman Prescription Drug
Proprietary NameBumetanide
Generic NameBumetanide
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2007-10-16
Marketing CategoryANDA / ANDA
Application NumberANDA074225
Labeler NameNCS HealthCare of KY, Inc dba Vangard Labs
Substance NameBUMETANIDE
Active Ingredient Strength1 mg/1
Pharm ClassesLoop Diuretic [EPC],Increased Diuresis at Loop of Henle [PE]
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 0615-4536-31

31 TABLET in 1 BLISTER PACK (0615-4536-31)
Marketing Start Date2007-10-16
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0615-4536-31 [00615453631]

Bumetanide TABLET
Marketing CategoryANDA
Application NumberANDA074225
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2007-10-16
Inactivation Date2020-01-31

NDC 0615-4536-39 [00615453639]

Bumetanide TABLET
Marketing CategoryANDA
Application NumberANDA074225
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2007-10-16
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
BUMETANIDE1 mg/1

OpenFDA Data

SPL SET ID:925b309a-8a0b-4bcd-bdf4-1ec42780ecc2
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 197418
  • 197419

    • Pharmacological Class

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