NDC 51662-1291-01
This exact product or package identity exists in FDA auxiliary data but is not present in the current primary NDC product table. The package identity is preserved; status rows are reported source observations, not medical conclusions.
- Requested NDC
- 51662-1291-01
- Product root
- 51662-1291
- Identity scope
- Package
- Primary current NDC product row
- Not present
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Captured / source date | Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Archive | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|---|
| 2019-12-08 06:16 UTC · source 2019-12-05 | excluded package | package | 51662-1291 | 51662-1291-1 | Y | Unknown FDA exclusion code: Y | excluded / ndc_excluded.zip | 110d247fa046… | a55b01930146… |
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 HCI | DOPAMINE HCI | HF Acquisition Co LLC, DBA HealthFirst | 763d2b07-9cea-782e-e053-2a91aa0adc01 | 2024-02-22 | Warnings, Adverse reactions | 51662-1291 51662129101 |