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
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code71872-7066
Application NumberNDA018132
Product Classification
M
Marketing Category
C73594
G
Generic Name
Dopamine Hydrochloride
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateMay 30, 2023
FDA Product Classification
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