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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| NUPRO Chlorhexidine Gluconate | CHLORHEXIDINE GLUCONATE | Dentsply LLC. Professional Division Trading as "DENTSPLY Professional" | d9d25abd-c3b4-4713-91c7-538f98e8fb70 | 2024-12-24 | Warnings, Adverse reactions | MOR84MUD8E |
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| Base Laboratories Saline | SODIUM CHLORIDE | Joonem LLC | ba0868f6-d3de-40e2-bcb3-144fa53062c7 | 2024-12-23 | Warnings | 451W47IQ8X |
| Base Laboratories Saline | SODIUM CHLORIDE | Joonem LLC | 9d83f477-ebbc-4248-8445-769178181d4f | 2024-12-23 | Warnings | 451W47IQ8X |
| Hibiclens | CHLORHEXIDINE GLUCONATE | Molnlycke Health Care | 29b547bf-c08e-14c2-e054-00144ff88e88 | 2024-12-23 | Warnings | MOR84MUD8E |
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| Hibiclens | CHLORHEXIDINE GLUCONATE | Molnlycke Health Care | 8b37a721-79bb-4051-95a7-fcb4edebfcb7 | 2024-12-23 | Warnings | MOR84MUD8E |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.