USFDA APPLICATION NUMBER - 22260 / DOSAGE - INJECTABLE;INJECTION - EQ 1.5MG BASE/VIAL
Active Ingredient/Active Moiety | ||
Ingredient Name | Basis of Strength | Strength |
---|---|---|
epoprostenol sodium(UNII: 4K04IQ1OF4) (epoprostenol - UNII:DCR9Z582X0) | epoprostenol sodium | 15000ng in 10 |
Inactive Ingredients
Ingredient Name | Actelion Pharmaceuticals US, Inc. | Jubilant HollisterStier General Partnership | Sun Pharmaceutical Industries, Inc. | Teva Parenteral Medicines, Inc. |
---|---|---|---|---|
ARGININE(94ZLA3W45F) | ||||
GLYCINE(TE7660XO1C) | ||||
MANNITOL(3OWL53L36A) | ||||
SODIUM CHLORIDE(451W47IQ8X) | ||||
SODIUM HYDROXIDE(55X04QC32I) | ||||
SUCROSE(C151H8M554) |
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