USFDA APPLICATION NUMBER - 21131 / DOSAGE - SOLUTION;INTRAVENOUS - 400MG/200ML (2MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
---|---|---|
LINEZOLID(UNII: ISQ9I6J12J) (LINEZOLID - UNII:ISQ9I6J12J) | LINEZOLID | 600mg in 300 |
Inactive Ingredients
Ingredient Name | Fresenius Kabi Norge As |
---|---|
CITRIC ACID MONOHYDRATE(2968PHW8QP) | |
DEXTROSE, UNSPECIFIED FORM(IY9XDZ35W2) | |
SODIUM CITRATE, UNSPECIFIED FORM(1Q73Q2JULR) |
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