Furosemide
FUROSEMIDE TABLETS USP
Approved
Approval ID
54410c7f-83a9-4797-9f81-7ca568130298
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 9, 2010
Manufacturers
FDA
Contract Pharmacy Services-PA
DUNS: 945429777
Products 1
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 Code67046-221
Application NumberANDA018413
Product Classification
M
Marketing Category
C73584
G
Generic Name
Furosemide
Product Specifications
Route of AdministrationORAL
Effective DateMarch 2, 2009
FDA Product Classification
INGREDIENTS (7)
FurosemideActive
Quantity: 40 mg in 1 1
Code: 7LXU5N7ZO5
Classification: ACTIB
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
POVIDONEInactive
Code: FZ989GH94E
Classification: IACT
LACTOSE MONOHYDRATEInactive
Code: EWQ57Q8I5X
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
SODIUM STARCH GLYCOLATE TYPE A POTATOInactive
Code: 5856J3G2A2
Classification: IACT