MedPath

Furosemide

Furosemide Tablets, USP

Approved
Approval ID

802fda1f-cfa7-422c-8d5b-e9b83a3f02d0

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Jun 13, 2011

Manufacturers
FDA

McKesson Packaging Services Business Unit of McKesson Corporation

DUNS: 140529962

Products 3

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Furosemide

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code63739-113
Application NumberANDA018569
Product Classification
M
Marketing Category
C73584
G
Generic Name
Furosemide
Product Specifications
Route of AdministrationORAL
Effective DateJanuary 17, 2008
FDA Product Classification

INGREDIENTS (4)

FUROSEMIDEActive
Quantity: 80 mg in 1 1
Code: 7LXU5N7ZO5
Classification: ACTIB
LACTOSE MONOHYDRATEInactive
Code: EWQ57Q8I5X
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT

Furosemide

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code63739-111
Application NumberANDA018569
Product Classification
M
Marketing Category
C73584
G
Generic Name
Furosemide
Product Specifications
Route of AdministrationORAL
Effective DateJanuary 17, 2008
FDA Product Classification

INGREDIENTS (4)

FUROSEMIDEActive
Quantity: 20 mg in 1 1
Code: 7LXU5N7ZO5
Classification: ACTIB
LACTOSE MONOHYDRATEInactive
Code: EWQ57Q8I5X
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT

Furosemide

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code63739-112
Application NumberANDA018569
Product Classification
M
Marketing Category
C73584
G
Generic Name
Furosemide
Product Specifications
Route of AdministrationORAL
Effective DateJanuary 17, 2008
FDA Product Classification

INGREDIENTS (4)

FUROSEMIDEActive
Quantity: 40 mg in 1 1
Code: 7LXU5N7ZO5
Classification: ACTIB
LACTOSE MONOHYDRATEInactive
Code: EWQ57Q8I5X
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT

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Furosemide - FDA Drug Approval Details