NDC 23155-473

Furosemide

Furosemide

Furosemide is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Heritage Pharmaceuticals Inc. D/b/a Avet Pharmaceuticals Inc.. The primary component is Furosemide.

Product ID23155-473_518e42a7-fa6d-4d16-8732-0ef896a82fa4
NDC23155-473
Product TypeHuman Prescription Drug
Proprietary NameFurosemide
Generic NameFurosemide
Dosage FormInjection, Solution
Route of AdministrationINTRAVENOUS
Marketing Start Date2014-09-02
Marketing CategoryANDA / ANDA
Application NumberANDA203428
Labeler NameHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Substance NameFUROSEMIDE
Active Ingredient Strength10 mg/mL
Pharm ClassesIncreased Diuresis at Loop of Henle [PE], Loop Diuretic [EPC]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 23155-473-41

25 VIAL in 1 CARTON (23155-473-41) > 2 mL in 1 VIAL (23155-473-31)
Marketing Start Date2014-09-02
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 23155-473-42 [23155047342]

Furosemide INJECTION, SOLUTION
Marketing CategoryANDA
Application NumberANDA203428
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2014-09-02

NDC 23155-473-43 [23155047343]

Furosemide INJECTION, SOLUTION
Marketing CategoryANDA
Application NumberANDA203428
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-09-02

NDC 23155-473-45 [23155047345]

Furosemide INJECTION, SOLUTION
Marketing CategoryANDA
Application NumberANDA203428
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-09-02

NDC 23155-473-31 [23155047331]

Furosemide INJECTION, SOLUTION
Marketing CategoryANDA
Application NumberANDA203428
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2014-09-02

NDC 23155-473-41 [23155047341]

Furosemide INJECTION, SOLUTION
Marketing CategoryANDA
Application NumberANDA203428
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2014-09-02

NDC 23155-473-33 [23155047333]

Furosemide INJECTION, SOLUTION
Marketing CategoryANDA
Application NumberANDA203428
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2014-09-02

NDC 23155-473-44 [23155047344]

Furosemide INJECTION, SOLUTION
Marketing CategoryANDA
Application NumberANDA203428
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2014-09-02

NDC 23155-473-32 [23155047332]

Furosemide INJECTION, SOLUTION
Marketing CategoryANDA
Application NumberANDA203428
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2014-09-02

Drug Details

Active Ingredients

IngredientStrength
FUROSEMIDE10 mg/mL

OpenFDA Data

SPL SET ID:1b9117d5-0dd9-4577-a1fd-bb0aaf7e68ec
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1719286
  • 1719290
  • 1719291
  • 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.