xylocaine
Generic: lidocaine hydrochloride
Labeler: asclemed usa incDrug Facts
Product Profile
Brand Name
xylocaine
Generic Name
lidocaine hydrochloride
Labeler
asclemed usa inc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
lidocaine hydrochloride anhydrous 20 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
76420-408
Product ID
76420-408_38554279-13f5-31f0-e063-6294a90a81a5
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA006488
Listing Expiration
2026-12-31
Marketing Start
2010-08-12
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
76420408
Hyphenated Format
76420-408
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 (76420-408-10)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INFILTRATION", "PERINEURAL"], "spl_id": "38554279-13f5-31f0-e063-6294a90a81a5", "openfda": {"unii": ["EC2CNF7XFP"], "rxcui": ["1010671", "1010673"], "spl_set_id": ["24e7b8b6-2de2-466d-ae2e-5eba8b2bc754"], "manufacturer_name": ["ASCLEMED USA INC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 mL in 1 VIAL, MULTI-DOSE (76420-408-10)", "package_ndc": "76420-408-10", "marketing_start_date": "20250620"}], "brand_name": "Xylocaine", "product_id": "76420-408_38554279-13f5-31f0-e063-6294a90a81a5", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "76420-408", "generic_name": "LIDOCAINE HYDROCHLORIDE", "labeler_name": "ASCLEMED USA INC", "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": "20261231"}