lidocaine hydrochloride
Generic: lidocaine hydrochloride
Labeler: sportpharm llcDrug Facts
Product Profile
Brand Name
lidocaine hydrochloride
Generic Name
lidocaine hydrochloride
Labeler
sportpharm llc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
lidocaine hydrochloride 20 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
85766-014
Product ID
85766-014_49ef1f9e-2cea-bcbb-e063-6394a90a82fa
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA207182
Listing Expiration
2027-12-31
Marketing Start
2017-10-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
85766014
Hyphenated Format
85766-014
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
ANDA207182 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/mL
Packaging
- 25 VIAL, MULTI-DOSE in 1 CARTON (85766-014-20) / 20 mL in 1 VIAL, MULTI-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INFILTRATION", "PERINEURAL"], "spl_id": "49ef1f9e-2cea-bcbb-e063-6394a90a82fa", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1010671"], "spl_set_id": ["415a29c1-101a-4ac2-9ba9-b419a1ce5600"], "manufacturer_name": ["Sportpharm LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, MULTI-DOSE in 1 CARTON (85766-014-20) / 20 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "85766-014-20", "marketing_start_date": "20250620"}], "brand_name": "Lidocaine Hydrochloride", "product_id": "85766-014_49ef1f9e-2cea-bcbb-e063-6394a90a82fa", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "85766-014", "generic_name": "Lidocaine Hydrochloride", "labeler_name": "Sportpharm LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lidocaine Hydrochloride", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA207182", "marketing_category": "ANDA", "marketing_start_date": "20171030", "listing_expiration_date": "20271231"}