lidocaine hydrochloride
Generic: lidocaine hydrochloride
Labeler: asclemed usa, inc.Drug Facts
Product Profile
Brand Name
lidocaine hydrochloride
Generic Name
lidocaine hydrochloride
Labeler
asclemed usa, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
lidocaine hydrochloride 10 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
76420-084
Product ID
76420-084_ead317e5-93f1-fd8d-e053-2995a90adbf6
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA080408
Listing Expiration
2026-12-31
Marketing Start
2005-07-08
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
76420084
Hyphenated Format
76420-084
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
lidocaine hydrochloride (source: ndc)
Generic Name
lidocaine hydrochloride (source: ndc)
Application Number
ANDA080408 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/mL
Packaging
- 2 mL in 1 AMPULE (76420-084-02)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["EPIDURAL", "INFILTRATION", "INTRACAUDAL", "PERINEURAL"], "spl_id": "ead317e5-93f1-fd8d-e053-2995a90adbf6", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1737568"], "spl_set_id": ["deec52c7-ebcf-422e-beab-bc1df2fe30cb"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "2 mL in 1 AMPULE (76420-084-02)", "package_ndc": "76420-084-02", "marketing_start_date": "20200506"}], "brand_name": "Lidocaine Hydrochloride", "product_id": "76420-084_ead317e5-93f1-fd8d-e053-2995a90adbf6", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "76420-084", "generic_name": "LIDOCAINE HYDROCHLORIDE", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lidocaine Hydrochloride", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "ANDA080408", "marketing_category": "ANDA", "marketing_start_date": "20050708", "listing_expiration_date": "20261231"}