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21572 / DOSAGE - POWDER;INTRAVENOUS - 500MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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) |
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