USFDA APPLICATION NUMBER - 20509 / DOSAGE - INJECTABLE;INJECTION - EQ 200MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
---|---|---|
Gemcitabine hydrochloride(UNII: U347PV74IL) (Gemcitabine - UNII:B76N6SBZ8R) | Gemcitabine | 1g in 25 | 200mg in 5 |
Inactive Ingredients
Ingredient Name | Eli Lilly and Company |
---|---|
Hydrochloric acid(QTT17582CB) | |
Mannitol(3OWL53L36A) | |
Sodium acetate(4550K0SC9B) | |
Sodium hydroxide(55X04QC32I) |
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