NDC 51688-6010 - SINGLE SHOT EPIDURAL 17G TUOHY A3771-17
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
- 51688-6010
- Package NDCs from labels
- 51688-6010-2
- Manufacturer
- Smiths Medical ASD, Inc. | Aplicare, Inc.
- Effective date
- 2011-06-03
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Regional Anesthesia Kit - Smiths Medical ASD, Inc. | Aplicare, Inc. | Smiths Medical ASD, Inc. | Aplicare, Inc. | 2011-06-03 | MEDICAL DEVICE |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| POVIDONE-IODINE | ACTIVE INGREDIENT | 85H0HZU99M | SINGLE SHOT EPIDURAL 17G TUOHY (REGIONAL ANESTHESIA KIT) KIT [SMITHS MEDICAL ASD, INC.] | 6 | |
| IODINE | ACTIVE MOIETY | 9679TC07X4 | SINGLE SHOT EPIDURAL 17G TUOHY (REGIONAL ANESTHESIA KIT) KIT [SMITHS MEDICAL ASD, INC.] | 6 | |
| CITRIC ACID MONOHYDRATE | INACTIVE INGREDIENT | 2968PHW8QP | SINGLE SHOT EPIDURAL 17G TUOHY (REGIONAL ANESTHESIA KIT) KIT [SMITHS MEDICAL ASD, INC.] | 6 | |
| NONOXYNOL-9 | INACTIVE INGREDIENT | 48Q180SH9T | SINGLE SHOT EPIDURAL 17G TUOHY (REGIONAL ANESTHESIA KIT) KIT [SMITHS MEDICAL ASD, INC.] | 6 | |
| SODIUM HYDROXIDE | INACTIVE INGREDIENT | 55X04QC32I | SINGLE SHOT EPIDURAL 17G TUOHY (REGIONAL ANESTHESIA KIT) KIT [SMITHS MEDICAL ASD, INC.] | 6 | |
| SODIUM PHOSPHATE, DIBASIC | INACTIVE INGREDIENT | GR686LBA74 | SINGLE SHOT EPIDURAL 17G TUOHY (REGIONAL ANESTHESIA KIT) KIT [SMITHS MEDICAL ASD, INC.] | 6 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | SINGLE SHOT EPIDURAL 17G TUOHY (REGIONAL ANESTHESIA KIT) KIT [SMITHS MEDICAL ASD, INC.] | 6 |
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 |
|---|---|---|---|---|---|---|
| Sterile Water | WATER | Baxter Healthcare Company | 210dc9ab-d6ca-4552-ac19-1be17792d290 | 2016-05-31 | Warnings, Adverse reactions | 059QF0KO0R |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.