NDC 36000-284

FUROSEMIDE

Furosemide

FUROSEMIDE is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Baxter Healthcare Corporation. The primary component is Furosemide.

Product ID36000-284_9b368371-dab6-496c-9417-5f5286f0c4e6
NDC36000-284
Product TypeHuman Prescription Drug
Proprietary NameFUROSEMIDE
Generic NameFurosemide
Dosage FormInjection, Solution
Route of AdministrationINTRAVENOUS
Marketing Start Date2014-02-06
Marketing CategoryANDA / ANDA
Application NumberANDA202747
Labeler NameBaxter Healthcare Corporation
Substance NameFUROSEMIDE
Active Ingredient Strength10 mg/mL
Pharm ClassesIncreased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 36000-284-25

25 VIAL, GLASS in 1 BOX (36000-284-25) > 10 mL in 1 VIAL, GLASS
Marketing Start Date2014-02-06
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 36000-284-25 [36000028425]

FUROSEMIDE INJECTION, SOLUTION
Marketing CategoryANDA
Application NumberANDA202747
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2014-02-06

Drug Details

Active Ingredients

IngredientStrength
FUROSEMIDE10 mg/mL

OpenFDA Data

SPL SET ID:c71371a7-75c5-45b8-b762-8d782d4c71bc
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1719286
  • 1719290
  • 1719291
  • UPC Code
  • 0336000065016
  • 0336000284257
  • 0336000283250
  • 0336000064019
  • 0336000063012
  • Pharmacological Class

    • 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.