lidocaine
Generic: lidocaine
Labeler: direct_rxDrug Facts
Product Profile
Brand Name
lidocaine
Generic Name
lidocaine
Labeler
direct_rx
Dosage Form
OINTMENT
Routes
Active Ingredients
lidocaine 50 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
72189-499
Product ID
72189-499_2c4e4735-85f2-83d7-e063-6394a90adcc0
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA206498
Listing Expiration
2026-12-31
Marketing Start
2023-07-14
Pharmacologic Class
Established (EPC)
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72189499
Hyphenated Format
72189-499
Supplemental Identifiers
RxCUI
UNII
NUI
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 (source: ndc)
Application Number
ANDA206498 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/g
Packaging
- 50 g in 1 JAR (72189-499-50)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "2c4e4735-85f2-83d7-e063-6394a90adcc0", "openfda": {"nui": ["N0000175682", "M0000897", "N0000175426", "N0000175976"], "unii": ["98PI200987"], "rxcui": ["1543069"], "spl_set_id": ["00725e5b-694c-b9e1-e063-6294a90a4182"], "pharm_class_cs": ["Amides [CS]"], "pharm_class_pe": ["Local Anesthesia [PE]"], "pharm_class_epc": ["Amide Local Anesthetic [EPC]", "Antiarrhythmic [EPC]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "50 g in 1 JAR (72189-499-50)", "package_ndc": "72189-499-50", "marketing_start_date": "20230714"}], "brand_name": "Lidocaine", "product_id": "72189-499_2c4e4735-85f2-83d7-e063-6394a90adcc0", "dosage_form": "OINTMENT", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "72189-499", "generic_name": "Lidocaine", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lidocaine", "active_ingredients": [{"name": "LIDOCAINE", "strength": "50 mg/g"}], "application_number": "ANDA206498", "marketing_category": "ANDA", "marketing_start_date": "20230714", "listing_expiration_date": "20261231"}