USFDA APPLICATION NUMBER - 210737 / DOSAGE - SOLUTION;SUBCUTANEOUS - 20MG/0.8ML (20MG/0.8ML)
Active Ingredient/Active Moiety | ||
Ingredient Name | Basis of Strength | Strength |
---|---|---|
methotrexate(UNII: YL5FZ2Y5U1) (methotrexate - UNII:YL5FZ2Y5U1) | methotrexate | 25mg in 1 | 22.5mg in 0.9 | 7.5mg in 0.3 | 10mg in 0.4 | 12.5mg in 0.5 | 20mg in 0.8 | 17.5mg in 0.7 | 15mg in 0.6 |
Inactive Ingredients
Ingredient Name | Cumberland Pharmaceuticals Inc. |
---|---|
sodium chloride(451W47IQ8X) | |
sodium hydroxide(55X04QC32I) | |
water(059QF0KO0R) |
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