Furosemide
FUROSEMIDE TABLETS USP
Approved
Approval ID
a10def90-97c4-43dc-9312-496b8ad89dab
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jun 3, 2014
Manufacturers
FDA
Cardinal Health
DUNS: 188557102
Products 2
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 Code55154-6328
Application NumberANDA018413
Product Classification
M
Marketing Category
C73584
G
Generic Name
Furosemide
Product Specifications
Route of AdministrationORAL
Effective DateJune 3, 2014
FDA Product Classification
INGREDIENTS (7)
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
magnesium stearateInactive
Code: 70097M6I30
Classification: IACT
FurosemideActive
Quantity: 20 mg in 1 1
Code: 7LXU5N7ZO5
Classification: ACTIB
lactose monohydrateInactive
Code: EWQ57Q8I5X
Classification: IACT
POVIDONESInactive
Code: FZ989GH94E
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
SODIUM STARCH GLYCOLATE TYPE A POTATOInactive
Code: 5856J3G2A2
Classification: IACT
Furosemide
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code55154-6330
Application NumberANDA018413
Product Classification
M
Marketing Category
C73584
G
Generic Name
Furosemide
Product Specifications
Route of AdministrationORAL
Effective DateJune 3, 2014
FDA Product Classification
INGREDIENTS (7)
SODIUM STARCH GLYCOLATE TYPE A POTATOInactive
Code: 5856J3G2A2
Classification: IACT
FurosemideActive
Quantity: 40 mg in 1 1
Code: 7LXU5N7ZO5
Classification: ACTIB
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
lactose monohydrateInactive
Code: EWQ57Q8I5X
Classification: IACT
magnesium stearateInactive
Code: 70097M6I30
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
POVIDONESInactive
Code: FZ989GH94E
Classification: IACT