lidocaine hydrochloride
Generic: lidocaine hydrochloride
Labeler: eugia us llcDrug Facts
Product Profile
Brand Name
lidocaine hydrochloride
Generic Name
lidocaine hydrochloride
Labeler
eugia us llc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
lidocaine hydrochloride 20 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
55150-254
Product ID
55150-254_ccc38d8a-43fd-44c0-985e-32af9ed956ab
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA207182
Listing Expiration
2026-12-31
Marketing Start
2017-10-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
55150254
Hyphenated Format
55150-254
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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 (55150-254-24) / 10 mL in 1 VIAL, MULTI-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (2)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INFILTRATION", "PERINEURAL"], "spl_id": "ccc38d8a-43fd-44c0-985e-32af9ed956ab", "openfda": {"upc": ["0355150252244", "0355150251247", "0355150255245", "0355150254248"], "unii": ["V13007Z41A"], "rxcui": ["1010033", "1010671"], "spl_set_id": ["ccc38d8a-43fd-44c0-985e-32af9ed956ab"], "manufacturer_name": ["Eugia US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, MULTI-DOSE in 1 CARTON (55150-254-24) / 10 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "55150-254-24", "marketing_start_date": "20171030"}], "brand_name": "Lidocaine Hydrochloride", "product_id": "55150-254_ccc38d8a-43fd-44c0-985e-32af9ed956ab", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "55150-254", "generic_name": "Lidocaine Hydrochloride", "labeler_name": "Eugia US 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": "20261231"}