lidocaine hydrochloride
Generic: lidocaine hydrochloride
Labeler: aurobindo pharma limitedDrug Facts
Product Profile
Brand Name
lidocaine hydrochloride
Generic Name
lidocaine hydrochloride
Labeler
aurobindo pharma limited
Dosage Form
SOLUTION
Routes
Active Ingredients
lidocaine hydrochloride 20 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
59651-943
Product ID
59651-943_ab461805-413a-4fb3-88a1-224e1c423084
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA219759
Listing Expiration
2026-12-31
Marketing Start
2025-07-29
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
59651943
Hyphenated Format
59651-943
Supplemental Identifiers
RxCUI
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
ANDA219759 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/mL
Packaging
- 100 mL in 1 BOTTLE (59651-943-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL", "TOPICAL"], "spl_id": "ab461805-413a-4fb3-88a1-224e1c423084", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1010739"], "spl_set_id": ["ab461805-413a-4fb3-88a1-224e1c423084"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (59651-943-01)", "package_ndc": "59651-943-01", "marketing_start_date": "20250729"}], "brand_name": "LIDOCAINE HYDROCHLORIDE", "product_id": "59651-943_ab461805-413a-4fb3-88a1-224e1c423084", "dosage_form": "SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "59651-943", "generic_name": "Lidocaine Hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LIDOCAINE HYDROCHLORIDE", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA219759", "marketing_category": "ANDA", "marketing_start_date": "20250729", "listing_expiration_date": "20261231"}