Furosemide
Approved
Approval ID
e8641b3c-5ab9-4e76-8e28-e9cadca8ec4a
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Feb 4, 2023
Manufacturers
FDA
A-S Medication Solutions
DUNS: 830016429
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 Code50090-2560
Application NumberNDA018487
Product Classification
M
Marketing Category
C73594
G
Generic Name
furosemide
Product Specifications
Route of AdministrationORAL
Effective DateJune 28, 2018
FDA Product Classification
INGREDIENTS (6)
FUROSEMIDEActive
Quantity: 20 mg in 1 1
Code: 7LXU5N7ZO5
Classification: ACTIB
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
MICROCRYSTALLINE CELLULOSEInactive
Code: OP1R32D61U
Classification: IACT
LACTOSE MONOHYDRATEInactive
Code: EWQ57Q8I5X
Classification: IACT
STEARIC ACIDInactive
Code: 4ELV7Z65AP
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT