NDC 51688-9282 - A3265-18 SINGLE SHOT EPIDURAL
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
- 51688-9282
- Package NDCs from labels
- 51688-9282-2
- Manufacturer
- Smiths Medical ASD, Inc. | Hospira, Inc. | Kwang Myung Pharm. Co., Ltd.
- Effective date
- 2016-07-08
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| A3265-18 SINGLE SHOT EPIDURAL | Smiths Medical ASD, Inc. | Hospira, Inc. | Kwang Myung Pharm. Co., Ltd. | 2016-07-08 | MEDICAL DEVICE |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| LIDOCAINE HYDROCHLORIDE | ACTIVE INGREDIENT | V13007Z41A | A3265-18 SINGLE SHOT EPIDURAL () KIT [SMITHS MEDICAL ASD, INC.] | 4 | |
| SODIUM CHLORIDE | ACTIVE INGREDIENT | 451W47IQ8X | A3265-18 SINGLE SHOT EPIDURAL () KIT [SMITHS MEDICAL ASD, INC.] | 4 | |
| LIDOCAINE | ACTIVE MOIETY | 98PI200987 | A3265-18 SINGLE SHOT EPIDURAL () KIT [SMITHS MEDICAL ASD, INC.] | 4 | |
| SODIUM CATION | ACTIVE MOIETY | LYR4M0NH37 | A3265-18 SINGLE SHOT EPIDURAL () KIT [SMITHS MEDICAL ASD, INC.] | 4 | |
| HYDROCHLORIC ACID | INACTIVE INGREDIENT | QTT17582CB | A3265-18 SINGLE SHOT EPIDURAL () KIT [SMITHS MEDICAL ASD, INC.] | 4 | |
| SODIUM CHLORIDE | INACTIVE INGREDIENT | 451W47IQ8X | A3265-18 SINGLE SHOT EPIDURAL () KIT [SMITHS MEDICAL ASD, INC.] | 4 | |
| SODIUM HYDROXIDE | INACTIVE INGREDIENT | 55X04QC32I | A3265-18 SINGLE SHOT EPIDURAL () KIT [SMITHS MEDICAL ASD, INC.] | 4 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | A3265-18 SINGLE SHOT EPIDURAL () KIT [SMITHS MEDICAL ASD, INC.] | 4 |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.