NDC 46066-222 - LIDOCAINE
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
- 46066-222
- Package NDCs from labels
- 46066-222-04, 46066-222-05
- Manufacturer
- Aspen Veterinary Resources, Ltd.
- Effective date
- 2019-05-31
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| LIDOCAINE INJECTION Local Anesthetic | Aspen Veterinary Resources, Ltd. | 2019-05-31 | PRESCRIPTION ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 46066-222-04 | LIDOCAINE | 100 mL in 1 BOTTLE | INJECTION | 100 | 5 | |
| 46066-222-05 | LIDOCAINE | 250 mL in 1 BOTTLE | INJECTION | 250 | 5 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| LIDOCAINE HYDROCHLORIDE | ACTIVE INGREDIENT | V13007Z41A | LIDOCAINE INJECTION [ASPEN VETERINARY RESOURCES, LTD.] | 3 | |
| LIDOCAINE | ACTIVE MOIETY | 98PI200987 | LIDOCAINE INJECTION [ASPEN VETERINARY RESOURCES, LTD.] | 3 |
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 |
|---|---|---|---|---|---|---|
| First Aid Burn | BENZALKONIUM CHLORIDE, LIDOCAINE HYDROCHLORIDE | Water-Jel Technologies | 25ebf112-8ac3-4402-9a87-00e454ab7efa | 2017-11-30 | Warnings | V13007Z41A |
| CVS Pain Relieving First Aid Antiseptic | LIDOCAINE HYDROCHLORIDE, BENZALKONIUM CHLORIDE | CVS Pharmacy | 454b1773-eda8-5610-e054-00144ff88e88 | 2017-01-04 | Warnings | V13007Z41A |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.