FDA Product

Furosemide

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

Basic Information

Product Name

Furosemide

FDA Product Code

0904-7178

Regulatory Information

NDC Product Code

0904-7178

Application Number

ANDA076796

Marketing Category

C73584

Effective Date

December 30, 2021

Territorial Authority

USA

FDA Title

FUROSEMIDE TABLETS, USP 20, 40, and 80 mg

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Version Number

1

Company Information

ManufacturerMajor Pharmaceuticals

DUNS Number

191427277

Active Ingredients

Quantity: 40 mg in 1 1

Code: 7LXU5N7ZO5

Class Code: ACTIB

LACTOSE MONOHYDRATE

Code: EWQ57Q8I5X

Class Code: IACT

STARCH, CORN

Code: O8232NY3SJ

Class Code: IACT

MAGNESIUM STEARATE

Code: 70097M6I30

Class Code: IACT

TALC

Code: 7SEV7J4R1U

Class Code: IACT

Active Moieties

FUROSEMIDE

Code: 7LXU5N7ZO5

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