Xylocaine MPF
NDC 63323-492, LIDOCAINE HYDROCHLORIDE, injection, solution, from Fresenius Kabi USA, LLC.
- Product NDC
- 63323-492
- Status
- Listed
- Labeler
- Fresenius Kabi USA, LLC
- Dosage form
- INJECTION, SOLUTION
- Route
- EPIDURAL, INFILTRATION, INTRACAUDAL, PERINEURAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA006488
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/63323-492 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- LIDOCAINE HYDROCHLORIDE ANHYDROUS10 mg/mL
Pharmacologic classes
Amide Local Anesthetic [EPC]; Amides [CS]; Antiarrhythmic [EPC]; Local Anesthesia [PE]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 63323-492-16 | 63323049216 | 25 VIAL, SINGLE-DOSE in 1 CARTON (63323-492-16) / 2 mL in 1 VIAL, SINGLE-DOSE (63323-492-41) |
| 63323-492-26 | 63323049226 | 25 VIAL, SINGLE-DOSE in 1 TRAY (63323-492-26) / 30 mL in 1 VIAL, SINGLE-DOSE (63323-492-45) |
| 63323-492-27 | 63323049227 | 25 VIAL, SINGLE-DOSE in 1 CARTON (63323-492-27) / 2 mL in 1 VIAL, SINGLE-DOSE (63323-492-04) |
| 63323-492-31 | 63323049231 | 5 VIAL, SINGLE-DOSE in 1 CARTON (63323-492-31) / 30 mL in 1 VIAL, SINGLE-DOSE (63323-492-03) |
| 63323-492-36 | 63323049236 | 25 VIAL, SINGLE-DOSE in 1 CARTON (63323-492-36) / 5 mL in 1 VIAL, SINGLE-DOSE (63323-492-43) |
| 63323-492-37 | 63323049237 | 25 VIAL, SINGLE-DOSE in 1 TRAY (63323-492-37) / 30 mL in 1 VIAL, SINGLE-DOSE (63323-492-07) |
| 63323-492-57 | 63323049257 | 25 VIAL, SINGLE-DOSE in 1 CARTON (63323-492-57) / 5 mL in 1 VIAL, SINGLE-DOSE (63323-492-09) |
| 63323-492-97 | 63323049297 | 5 AMPULE in 1 BOX (63323-492-97) / 10 mL in 1 AMPULE (63323-492-08) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels?ndc=63323-492
Use it
Look up 63323-492 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/63323-492 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 63323-492. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.