xylocaine mpf

Generic: lidocaine hydrochloride

Labeler: fresenius kabi usa, llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name xylocaine mpf
Generic Name lidocaine hydrochloride
Labeler fresenius kabi usa, llc
Dosage Form INJECTION, SOLUTION
Routes
EPIDURAL INFILTRATION INTRACAUDAL PERINEURAL
Active Ingredients

lidocaine hydrochloride anhydrous 10 mg/mL

Manufacturer
Fresenius Kabi USA, LLC

Identifiers & Regulatory

Product NDC 65219-810
Product ID 65219-810_db90b9bc-09cb-4f67-8cde-bd7fc1394d17
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA006488
Listing Expiration 2026-12-31
Marketing Start 2020-10-30

Pharmacologic Class

Classes
amide local anesthetic [epc] amides [cs] antiarrhythmic [epc] local anesthesia [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 65219810
Hyphenated Format 65219-810

Supplemental Identifiers

RxCUI
1737568 1737569 1737757 1737758 1737761 1737762
UPC
0365219814016 0365219812012 0365219810018
UNII
EC2CNF7XFP

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name xylocaine mpf (source: ndc)
Generic Name lidocaine hydrochloride (source: ndc)
Application Number NDA006488 (source: ndc)
Routes
EPIDURAL INFILTRATION INTRACAUDAL PERINEURAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/mL
source: ndc
Packaging
  • 25 VIAL, SINGLE-DOSE in 1 TRAY (65219-810-02) / 2 mL in 1 VIAL, SINGLE-DOSE (65219-810-01)
source: ndc

Packages (1)

65219-810-02 25 VIAL, SINGLE-DOSE in 1 TRAY (65219-810-02) / 2 mL in 1 VIAL, SINGLE-DOSE (65219-810-01)

Ingredients (1)

lidocaine hydrochloride anhydrous (10 mg/mL)

Linked Drug Pages (1)

Xylocaine MPF ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["EPIDURAL", "INFILTRATION", "INTRACAUDAL", "PERINEURAL"], "spl_id": "db90b9bc-09cb-4f67-8cde-bd7fc1394d17", "openfda": {"upc": ["0365219814016", "0365219812012", "0365219810018"], "unii": ["EC2CNF7XFP"], "rxcui": ["1737568", "1737569", "1737757", "1737758", "1737761", "1737762"], "spl_set_id": ["fe265eb5-eaeb-4f47-82dd-238c1d53fec4"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 TRAY (65219-810-02)  / 2 mL in 1 VIAL, SINGLE-DOSE (65219-810-01)", "package_ndc": "65219-810-02", "marketing_start_date": "20201030"}], "brand_name": "Xylocaine MPF", "product_id": "65219-810_db90b9bc-09cb-4f67-8cde-bd7fc1394d17", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "65219-810", "generic_name": "LIDOCAINE HYDROCHLORIDE", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Xylocaine", "brand_name_suffix": "MPF", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE ANHYDROUS", "strength": "10 mg/mL"}], "application_number": "NDA006488", "marketing_category": "NDA", "marketing_start_date": "20201030", "listing_expiration_date": "20261231"}