
USFDA APPLICATION NUMBER - 21572 / DOSAGE - POWDER;INTRAVENOUS - 500MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
|---|---|---|
| Daptomycin(UNII: NWQ5N31VKK) (Daptomycin - UNII:NWQ5N31VKK) | Daptomycin | 500mg in 10 |
Inactive Ingredients
| Ingredient Name | Merck Sharp & Dohme LLC | Teva Parenteral Medicines, Inc. |
|---|---|---|
| Sodium Hydroxide(55X04QC32I) | ||
| Sucrose(C151H8M554) |