FDA Product

Furosemide

Product approved by U.S. Food and Drug Administration (US)

Basic Information

Product Name

Furosemide

FDA Product Code

51655-310

Regulatory Information

NDC Product Code

51655-310

Application Number

ANDA076796

Marketing Category

C73584

Effective Date

January 20, 2023

Territorial Authority

USA

FDA Title

FUROSEMIDE TABLETS, USP 20mg

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Version Number

1

Company Information

ManufacturerNorthwind Pharmaceuticals, LLC

DUNS Number

036986393

Active Ingredients

Quantity: 20 mg in 1 1

Code: 7LXU5N7ZO5

Class Code: ACTIB

TALC

Code: 7SEV7J4R1U

Class Code: IACT

STARCH, CORN

Code: O8232NY3SJ

Class Code: IACT

LACTOSE MONOHYDRATE

Code: EWQ57Q8I5X

Class Code: IACT

MAGNESIUM STEARATE

Code: 70097M6I30

Class Code: IACT

Active Moieties

FUROSEMIDE

Code: 7LXU5N7ZO5

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