FDA.reportPublic FDA data

NDC 0409-7809-31 - Dopamine Hydrochloride in Dextrose

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
0409-7809
Requested NDC
0409-7809-31
Package NDCs from labels
0409-7809-11, 0409-7809-22, 0409-7809-31, 0409-7809-24
Manufacturer
Hospira, Inc.
Effective date
2026-05-12
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Dopamine Hydrochloride in Dextrose - Hospira, Inc.Hospira, Inc.2026-05-12HUMAN PRESCRIPTION DRUG LABEL
DOPAMINE HYDROCHLORIDE - HF Acquisition Co LLC, DBA HealthFirstHF Acquisition Co LLC, DBA HealthFirst2024-01-29HUMAN PRESCRIPTION DRUG LABEL
DOPAMINE HCI IN 5% DEXTROSE - HF Acquisition Co LLC, DBA HealthFirstHF Acquisition Co LLC, DBA HealthFirst2024-01-27HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0409-7809-11Dopamine Hydrochloride in Dextrose250 mL in 1 BAGINJECTION, SOLUTION25027
0409-7809-22Dopamine Hydrochloride in Dextrose12 in 1 CARTONINJECTION, SOLUTION1227
0409-7809-24Dopamine Hydrochloride in Dextrose12 in 1 CARTONINJECTION, SOLUTION1227
0409-7809-31Dopamine Hydrochloride in Dextrose500 mL in 1 BAGINJECTION, SOLUTION50027

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0409-7809DOPAMINE HYDROCHLORIDE IN DEXTROSE INJECTION, SOLUTION [HOSPIRA, INC.]23Current NDC, Legacy NDC, 4 package rows20241127_08f23f6e-150d-45ea-098e-f2edf64c21a1.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0409-7809-11ML - Milliliter0409-78090f5f70dd-c881-4534-ba67-7b1e9245d94c12019-08-06
0409-7809-22ML - Milliliter0409-780933d938a5-3c98-4dcc-9057-f90b1eaefc6d12013-02-13
0409-7809-24ML - Milliliter0409-78092c6e271f-0637-4254-bef2-50809e099c0912013-02-13
0409-7809-31ML - Milliliter0409-7809224c8f8e-53f6-489b-8d4c-e7b669bc797812019-08-06

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
DOPAMINE HYDROCHLORIDEACTIVE INGREDIENT7L3E358N9LDOPAMINE HYDROCHLORIDE AND DEXTROSE (DOPAMINE HYDROCHLORIDE) INJECTION, SOLUTION [HOSPIRA, INC.]12
DOPAMINEACTIVE MOIETYVTD58H1Z2XDOPAMINE HYDROCHLORIDE AND DEXTROSE (DOPAMINE HYDROCHLORIDE) INJECTION, SOLUTION [HOSPIRA, INC.]12
DEXTROSE MONOHYDRATEINACTIVE INGREDIENTLX22YL083GDOPAMINE HYDROCHLORIDE AND DEXTROSE (DOPAMINE HYDROCHLORIDE) INJECTION, SOLUTION [HOSPIRA, INC.]12
HYDROCHLORIC ACIDINACTIVE INGREDIENTQTT17582CBDOPAMINE HYDROCHLORIDE AND DEXTROSE (DOPAMINE HYDROCHLORIDE) INJECTION, SOLUTION [HOSPIRA, INC.]12
SODIUM HYDROXIDEINACTIVE INGREDIENT55X04QC32IDOPAMINE HYDROCHLORIDE AND DEXTROSE (DOPAMINE HYDROCHLORIDE) INJECTION, SOLUTION [HOSPIRA, INC.]12
SODIUM METABISULFITEINACTIVE INGREDIENT4VON5FNS3CDOPAMINE HYDROCHLORIDE AND DEXTROSE (DOPAMINE HYDROCHLORIDE) INJECTION, SOLUTION [HOSPIRA, INC.]12
WATERINACTIVE INGREDIENT059QF0KO0RDOPAMINE HYDROCHLORIDE AND DEXTROSE (DOPAMINE HYDROCHLORIDE) INJECTION, SOLUTION [HOSPIRA, INC.]12

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 19 of 19 · 363 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
DopamineDOPAMINE HYDROCHLORIDEBioActive Nutritional2e456b07-8b7b-463a-8cf5-1d7a51985b062016-08-16WarningsExact identifier
unii: 7L3E358N9L
Sterile WaterWATERBaxter Healthcare Company210dc9ab-d6ca-4552-ac19-1be17792d2902016-05-31Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
CPDA-1ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE ADENINEFenwal, Inc.051f7347-5a76-4664-8fe2-e61b3dfcb0e42014-08-27Exact identifier
unii: LX22YL083G

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.