xylocaine
Generic: lidocaine hydrochloride
Labeler: asclemed usa, inc.Drug 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
76420-369
Product ID
76420-369_366ad8d7-33a0-b252-e063-6294a90a7a16
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
76420369
Hyphenated Format
76420-369
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
- 25 VIAL, MULTI-DOSE in 1 TRAY (76420-369-25) / 10 mL in 1 VIAL, MULTI-DOSE (76420-369-10)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INFILTRATION", "PERINEURAL"], "spl_id": "366ad8d7-33a0-b252-e063-6294a90a7a16", "openfda": {"unii": ["EC2CNF7XFP"], "rxcui": ["1010671", "1010673"], "spl_set_id": ["25370b0f-0ac6-4a03-abe6-d73d65192180"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, MULTI-DOSE in 1 TRAY (76420-369-25) / 10 mL in 1 VIAL, MULTI-DOSE (76420-369-10)", "package_ndc": "76420-369-25", "marketing_start_date": "20250531"}], "brand_name": "Xylocaine", "product_id": "76420-369_366ad8d7-33a0-b252-e063-6294a90a7a16", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "76420-369", "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"}