get monetary savings solution Product Information Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:0409-7809 Route of Administration INTRAVENOUS DEA Schedule Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DOPAMINE HYDROCHLORIDE (DOPAMINE) DOPAMINE HYDROCHLORIDE 1.6 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER HYDROCHLORIC ACID SODIUM HYDROXIDE DEXTROSE MONOHYDRATE SODIUM METABISULFITE Packaging # Item Code Package Description 1 NDC:0409-7809-22 250 mL in 1 BAG 2 NDC:0409-7809-24 500 mL in 1 BAG Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA018826 04/30/2005 DOPAMINE HYDROCHLORIDE AND DEXTROSE dopamine hydrochloride injection on occasion
anticipating e Moiety Ingredient Name Basis of Strength Strength DOPAMINE HYDROCHLORIDE (DOPAMINE) DOPAMINE HYDROCHLORIDE 0.8 mg in 1 mL Inactive Ingredients Ingredient Name Strength DEXTROSE MONOHYDRATE WATER SODIUM METABISULFITE HYDROCHLORIC ACID SODIUM HYDROXIDE Packaging # Item Code Package Description 1 NDC:0409-7808-22 250 mL in 1 BAG 2 NDC:0409-7808-24 500 mL in 1 BAG Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA018826 06/21/2005 02/01/2018 DOPAMINE HYDROCHLORIDE AND DEXTROSE dopamine hydrochloride injection novices
EmoticonEmoticon