lydexa 4.12%
Generic: lidocaine hydrochloride
Labeler: puretek corporationDrug Facts
Product Profile
Brand Name
lydexa 4.12%
Generic Name
lidocaine hydrochloride
Labeler
puretek corporation
Dosage Form
CREAM
Routes
Active Ingredients
lidocaine hydrochloride 41.2 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
59088-429
Product ID
59088-429_d9450f79-6270-8222-e053-2a95a90a0a48
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
UNAPPROVED DRUG OTHER
Listing Expiration
2026-12-31
Marketing Start
2020-07-10
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
59088429
Hyphenated Format
59088-429
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
lydexa 4.12% (source: ndc)
Generic Name
lidocaine hydrochloride (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 41.2 mg/g
Packaging
- 1 TUBE in 1 CARTON (59088-429-03) / 28.3 g in 1 TUBE
- 1 TUBE in 1 CARTON (59088-429-07) / 85 g in 1 TUBE
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "d9450f79-6270-8222-e053-2a95a90a0a48", "openfda": {"upc": ["0359088429037"], "unii": ["V13007Z41A"], "rxcui": ["1947197", "2474489"], "spl_set_id": ["aa1c9d39-1283-8c6b-e053-2a95a90af5b5"], "manufacturer_name": ["PureTek Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (59088-429-03) / 28.3 g in 1 TUBE", "package_ndc": "59088-429-03", "marketing_start_date": "20200710"}, {"sample": false, "description": "1 TUBE in 1 CARTON (59088-429-07) / 85 g in 1 TUBE", "package_ndc": "59088-429-07", "marketing_start_date": "20220302"}], "brand_name": "Lydexa 4.12%", "product_id": "59088-429_d9450f79-6270-8222-e053-2a95a90a0a48", "dosage_form": "CREAM", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "59088-429", "generic_name": "Lidocaine Hydrochloride", "labeler_name": "PureTek Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lydexa 4.12%", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "41.2 mg/g"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20200710", "listing_expiration_date": "20261231"}