xylocaine
Generic: lidocaine hydrochloride
Labeler: sportpharm llcDrug Facts
Product Profile
Brand Name
xylocaine
Generic Name
lidocaine hydrochloride
Labeler
sportpharm llc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
lidocaine hydrochloride anhydrous 20 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
85766-018
Product ID
85766-018_49ef47ca-1c61-3bb9-e063-6294a90a6274
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA006488
Listing Expiration
2027-12-31
Marketing Start
2010-08-12
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
85766018
Hyphenated Format
85766-018
Supplemental Identifiers
RxCUI
UNII
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 (source: ndc)
Generic Name
lidocaine hydrochloride (source: ndc)
Application Number
NDA006488 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/mL
Packaging
- 10 mL in 1 VIAL, MULTI-DOSE (85766-018-10)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INFILTRATION", "PERINEURAL"], "spl_id": "49ef47ca-1c61-3bb9-e063-6294a90a6274", "openfda": {"unii": ["EC2CNF7XFP"], "rxcui": ["1010671", "1010673"], "spl_set_id": ["94155012-b1fc-430a-a1f5-30c21f4a3f80"], "manufacturer_name": ["Sportpharm LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 mL in 1 VIAL, MULTI-DOSE (85766-018-10)", "package_ndc": "85766-018-10", "marketing_start_date": "20250620"}], "brand_name": "Xylocaine", "product_id": "85766-018_49ef47ca-1c61-3bb9-e063-6294a90a6274", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "85766-018", "generic_name": "LIDOCAINE HYDROCHLORIDE", "labeler_name": "Sportpharm LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Xylocaine", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE ANHYDROUS", "strength": "20 mg/mL"}], "application_number": "NDA006488", "marketing_category": "NDA", "marketing_start_date": "20100812", "listing_expiration_date": "20271231"}