
USFDA APPLICATION NUMBER - 18579 / DOSAGE - INJECTABLE;INJECTION - 10MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
| Active Ingredient/Active Moiety | ||
| Ingredient Name | Basis of Strength | Strength | 
|---|---|---|
| furosemide(UNII: 7LXU5N7ZO5) (furosemide - UNII:7LXU5N7ZO5)  | furosemide | 20mg in 2 | 
Inactive Ingredients
| Ingredient Name | American Regent, Inc.  | Cardinal Health  | McKesson Packaging Services Business unit of McKesson Corporation  | 
					
|---|---|---|---|
| sodium chloride(451W47IQ8X) | |||
| water(059QF0KO0R) |