lidocaine hydrochloride
Generic: lidocaine hydrochloride
Labeler: pai holdings, llc dba pai pharmaDrug Facts
Product Profile
Brand Name
lidocaine hydrochloride
Generic Name
lidocaine hydrochloride
Labeler
pai holdings, llc dba pai pharma
Dosage Form
SOLUTION
Routes
Active Ingredients
lidocaine hydrochloride 20 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0121-0950
Product ID
0121-0950_8bd8bb07-066a-4c8c-ac5b-76f746318a49
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA218138
Listing Expiration
2026-12-31
Marketing Start
2024-02-20
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
01210950
Hyphenated Format
0121-0950
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
ANDA218138 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/mL
Packaging
- 12 BOTTLE in 1 CASE (0121-0950-03) / 100 mL in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8bd8bb07-066a-4c8c-ac5b-76f746318a49", "openfda": {"upc": ["0301210950032"], "unii": ["V13007Z41A"], "rxcui": ["1010739"], "spl_set_id": ["d5e23ede-957c-4a32-b1c6-268acb773c31"], "manufacturer_name": ["PAI Holdings, LLC dba PAI Pharma"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 BOTTLE in 1 CASE (0121-0950-03) / 100 mL in 1 BOTTLE", "package_ndc": "0121-0950-03", "marketing_start_date": "20240220"}], "brand_name": "Lidocaine Hydrochloride", "product_id": "0121-0950_8bd8bb07-066a-4c8c-ac5b-76f746318a49", "dosage_form": "SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "0121-0950", "generic_name": "Lidocaine Hydrochloride", "labeler_name": "PAI Holdings, LLC dba PAI Pharma", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lidocaine Hydrochloride", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA218138", "marketing_category": "ANDA", "marketing_start_date": "20240220", "listing_expiration_date": "20261231"}