lidocaine
Generic: lidocaine hydrochloride
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
lidocaine
Generic Name
lidocaine hydrochloride
Labeler
a-s medication solutions
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
lidocaine hydrochloride 20 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
50090-3366
Product ID
50090-3366_73ee82a6-0af2-4d3e-8ec1-32f158752f5b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA080407
Listing Expiration
2026-12-31
Marketing Start
1972-02-14
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500903366
Hyphenated Format
50090-3366
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 (source: ndc)
Generic Name
lidocaine hydrochloride (source: ndc)
Application Number
ANDA080407 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/mL
Packaging
- 1 VIAL, MULTI-DOSE in 1 PACKAGE (50090-3366-0) / 50 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": "73ee82a6-0af2-4d3e-8ec1-32f158752f5b", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1010671"], "spl_set_id": ["e6c83ad7-2821-432b-8610-0f54cfe610cb"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 PACKAGE (50090-3366-0) / 50 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "50090-3366-0", "marketing_start_date": "20180208"}], "brand_name": "Lidocaine", "product_id": "50090-3366_73ee82a6-0af2-4d3e-8ec1-32f158752f5b", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "50090-3366", "generic_name": "Lidocaine Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lidocaine", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA080407", "marketing_category": "ANDA", "marketing_start_date": "19720214", "listing_expiration_date": "20261231"}