Furosemide
Rx Only
Approved
Approval ID
0a105e0b-b5cc-d929-e063-6294a90a80af
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Nov 13, 2023
Manufacturers
FDA
Medical Purchasing Solutions, LLC
DUNS: 601458529
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 Code71872-7314
Application NumberANDA203428
Product Classification
M
Marketing Category
C73584
G
Generic Name
Furosemide
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateNovember 13, 2023
FDA Product Classification
INGREDIENTS (5)
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
HYDROCHLORIC ACIDInactive
Code: QTT17582CB
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
SODIUM HYDROXIDEInactive
Code: 55X04QC32I
Classification: IACT
FUROSEMIDEActive
Quantity: 10 mg in 1 mL
Code: 7LXU5N7ZO5
Classification: ACTIB