NDC 51688-6002 - Nerve Block A3769
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
- 51688-6002
- Package NDCs from labels
- 51688-6002-2
- Manufacturer
- Smiths Medical ASD, Inc. | CareFusion 213 LLC | Hospira, Inc.
- Effective date
- 2011-04-06
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Nerve Block A3769 | Smiths Medical ASD, Inc. | CareFusion 213 LLC | Hospira, Inc. | 2011-04-06 | MEDICAL DEVICE |
DailyMed Socrata Ingredients#
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.
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.