lidocaine hydrochloride

Generic: lidocaine hydrochloride

Labeler: eugia us llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lidocaine hydrochloride
Generic Name lidocaine hydrochloride
Labeler eugia us llc
Dosage Form INJECTION, SOLUTION
Routes
INFILTRATION PERINEURAL
Active Ingredients

lidocaine hydrochloride 10 mg/mL

Manufacturer
Eugia US LLC

Identifiers & Regulatory

Product NDC 55150-251
Product ID 55150-251_0b1f03c2-db2f-4f90-acc0-d73abd731bf6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207182
Listing Expiration 2026-12-31
Marketing Start 2017-10-30

Pharmacologic Class

Classes
amide local anesthetic [epc] amides [cs] antiarrhythmic [epc] local anesthesia [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 55150251
Hyphenated Format 55150-251

Supplemental Identifiers

RxCUI
1010033 1010671
UPC
0355150253500 0355150252206 0355150256501 0355150251100 0355150255207 0355150254101
UNII
V13007Z41A

Packaging Origin

Original Packager
true

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
INFILTRATION PERINEURAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/mL
source: ndc
Packaging
  • 25 VIAL, MULTI-DOSE in 1 CARTON (55150-251-10) / 10 mL in 1 VIAL, MULTI-DOSE
source: ndc

Packages (1)

55150-251-10 25 VIAL, MULTI-DOSE in 1 CARTON (55150-251-10) / 10 mL in 1 VIAL, MULTI-DOSE

Ingredients (1)

lidocaine hydrochloride (10 mg/mL)

Linked Drug Pages (2)

Lidocaine Hydrochloride ndc-match (0.9) Lidocaine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INFILTRATION", "PERINEURAL"], "spl_id": "0b1f03c2-db2f-4f90-acc0-d73abd731bf6", "openfda": {"upc": ["0355150253500", "0355150252206", "0355150256501", "0355150251100", "0355150255207", "0355150254101"], "unii": ["V13007Z41A"], "rxcui": ["1010033", "1010671"], "spl_set_id": ["ef782e5e-e2d7-465a-99c6-b12611f3158c"], "manufacturer_name": ["Eugia US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, MULTI-DOSE in 1 CARTON (55150-251-10)  / 10 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "55150-251-10", "marketing_start_date": "20171030"}], "brand_name": "Lidocaine Hydrochloride", "product_id": "55150-251_0b1f03c2-db2f-4f90-acc0-d73abd731bf6", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "55150-251", "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": "10 mg/mL"}], "application_number": "ANDA207182", "marketing_category": "ANDA", "marketing_start_date": "20171030", "listing_expiration_date": "20261231"}