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- 18579 / DOSAGE - INJECTABLE;INJECTION - 10MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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) |
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