furosemide
FUROSEMIDEINJECTION, USP10 mg/mL
Approved
Approval ID
3ec788b9-b851-4022-a3ef-8ec72bc3d258
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 28, 2010
Manufacturers
FDA
Rebel Distributors Corp
DUNS: 118802834
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 Code21695-721
Application NumberANDA018579
Product Classification
M
Marketing Category
C73584
G
Generic Name
furosemide
Product Specifications
Route of AdministrationINTRAVENOUS, INTRAMUSCULAR
Effective DateApril 13, 2006
FDA Product Classification
INGREDIENTS (3)
WATERInactive
Code: 059QF0KO0R
Classification: IACT
furosemideActive
Quantity: 10 mg in 2 mL
Code: 7LXU5N7ZO5
Classification: ACTIB
sodium chlorideInactive
Code: 451W47IQ8X
Classification: IACT