Furosemide
Furosemide Tablets, USP
Approved
Approval ID
918887d8-5c36-49e9-832d-d03a1d15f2a8
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Feb 11, 2011
Manufacturers
FDA
MedVantx, Inc.
DUNS: 806427725
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 Code66116-375
Application NumberANDA078010
Product Classification
M
Marketing Category
C73584
G
Generic Name
Furosemide
Product Specifications
Route of AdministrationORAL
Effective DateNovember 20, 2010
FDA Product Classification
INGREDIENTS (6)
LACTOSE MONOHYDRATEInactive
Code: EWQ57Q8I5X
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
FUROSEMIDEActive
Quantity: 40 mg in 1 1
Code: 7LXU5N7ZO5
Classification: ACTIB
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
SODIUM STARCH GLYCOLATE TYPE A POTATOInactive
Code: 5856J3G2A2
Classification: IACT