NDC 51662-1489-2 - DOPAMINE HYDROCHLORIDE
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
- 51662-1489
- Requested NDC
- 51662-1489-2
- Package NDCs from labels
- 51662-1489-1, 51662-1489-2, 51662-1489-3
- Manufacturer
- HF Acquisition Co LLC, DBA HealthFirst
- Effective date
- 2024-02-22
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| DOPAMINE HYDROCHLORIDE - HF Acquisition Co LLC, DBA HealthFirst | HF Acquisition Co LLC, DBA HealthFirst | 2024-02-22 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51662-1489-1 | DOPAMINE HYDROCHLORIDE | 5 mL in 1 VIAL, SINGLE-DOSE | INJECTION | 5 | 5 | |
| 51662-1489-2 | DOPAMINE HYDROCHLORIDE | 1 in 1 POUCH | INJECTION | 1 | 5 | |
| 51662-1489-2 | DOPAMINE HYDROCHLORIDE | 5 mL in 1 VIAL, SINGLE-DOSE | INJECTION | 5 | 5 | |
| 51662-1489-3 | DOPAMINE HYDROCHLORIDE | 25 in 1 CASE | INJECTION | 25 | 5 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 51662-1489 | DOPAMINE HYDROCHLORIDE INJECTION [HF ACQUISITION CO LLC, DBA HEALTHFIRST] | 5 | Current NDC, Legacy NDC, 4 package rows | 20240224_c901b461-4f98-da0a-e053-2a95a90a106e.zip |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Dopamine | DOPAMINE HYDROCHLORIDE | BioActive Nutritional | 2e456b07-8b7b-463a-8cf5-1d7a51985b06 | 2016-08-16 | Warnings | 7L3E358N9L |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.