USFDA APPLICATION NUMBER - 21264 / DOSAGE - INJECTABLE;SUBCUTANEOUS - 30MG/3ML (10MG/ML)
Active Ingredient/Active Moiety | ||
Ingredient Name | Basis of Strength | Strength |
---|---|---|
APOMORPHINE HYDROCHLORIDE(UNII: F39049Y068) (APOMORPHINE - UNII:N21FAR7B4S) | APOMORPHINE HYDROCHLORIDE | 30mg in 3 |
Inactive Ingredients
Ingredient Name | MDD US Operations, LLC | Tercica, Inc. |
---|---|---|
BENZYL ALCOHOL(LKG8494WBH) | ||
hydrochloric acid(QTT17582CB) | ||
sodium hydroxide(55X04QC32I) | ||
sodium metabisulfite(4VON5FNS3C) | ||
WATER(059QF0KO0R) |
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