FDA Label for Furosemide
View Indications, Usage & Precautions
Furosemide Product Label
The following document was submitted to the FDA by the labeler of this product Maiva Pharma Private Limited. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Warnings
Furosemide is a potent diuretic which, if given in excessive amounts, can lead to a profound diuresis with water and electrolyte depletion. Therefore, careful medical supervision is required and dose and dose schedule must be adjusted to the individual patient's needs. (See DOSAGE AND ADMINISTRATION.)
Package Label.Principal Display Panel
NDC 73542-101-01
Furosemide Injection, USP
20 mg/2 mL
(10 mglmL)
FOR IV OR IM USE
Rx only
2 mL Single-Dose vial
NDC 73542-101-25
Furosemide Injection, USP
20 mg/2 mL
(10 mglmL)
FOR IV OR IM USE
Rx only
25 Single-Dose vial
NDC 73542-102-02
Furosemide Injection, USP
40 mg/4 mL
(10 mglmL)
FOR IV OR IM USE
Rx only
4 mL Single-Dose vial
NDC 73542-102-25
Furosemide Injection, USP
40 mg/4 mL
(10 mglmL)
FOR IV OR IM USE
Rx only
25 Single-Dose via
NDC 73542-103-03
Furosemide Injection, USP
100 mg/10 mL
(10 mglmL)
FOR IV OR IM USE
Rx only
10 mL Single-Dose vial
NDC 73542-103-25
Furosemide Injection, USP
100 mg/10 mL
(10 mglmL)
FOR IV OR IM USE
Rx only
25 Single-Dose vial
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