DOPamine Hydrochloride
DOPamine HYDROCHLORIDE Rx only
Approved
Approval ID
b61fffd0-7bc8-09e2-e053-2995a90ae0e4
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
May 30, 2023
Manufacturers
FDA
Medical Purchasing Solutions, LLC
DUNS: 601458529
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Dopamine Hydrochloride
PRODUCT DETAILS
NDC Product Code71872-7066
Application NumberNDA018132
Marketing CategoryC73594
Route of AdministrationINTRAVENOUS
Effective DateMay 30, 2023
Generic NameDopamine Hydrochloride
INGREDIENTS (4)
SODIUM METABISULFITEInactive
Quantity: 9 mg in 1 mL
Code: 4VON5FNS3C
Classification: IACT
ANHYDROUS CITRIC ACIDInactive
Quantity: 10 mg in 1 mL
Code: XF417D3PSL
Classification: IACT
TRISODIUM CITRATE DIHYDRATEInactive
Quantity: 5 mg in 1 mL
Code: B22547B95K
Classification: IACT
DOPAMINE HYDROCHLORIDEActive
Quantity: 40 mg in 1 mL
Code: 7L3E358N9L
Classification: ACTIB