lidocaine hydrochloride
Generic: lidocaine hydrochloride
Labeler: propharma distributionDrug Facts
Product Profile
Brand Name
lidocaine hydrochloride
Generic Name
lidocaine hydrochloride
Labeler
propharma distribution
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
lidocaine hydrochloride 20 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
84549-323
Product ID
84549-323_463cf19d-84cc-608e-e063-6294a90a07bc
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA040302
Listing Expiration
2026-12-31
Marketing Start
2005-12-09
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
84549323
Hyphenated Format
84549-323
Supplemental Identifiers
RxCUI
UNII
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
ANDA040302 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/mL
Packaging
- 5 mL in 1 SYRINGE, PLASTIC (84549-323-05)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "463cf19d-84cc-608e-e063-6294a90a07bc", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1737761"], "spl_set_id": ["38560997-cfe4-2f9b-e063-6394a90a834b"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "5 mL in 1 SYRINGE, PLASTIC (84549-323-05)", "package_ndc": "84549-323-05", "marketing_start_date": "20250827"}], "brand_name": "Lidocaine Hydrochloride", "product_id": "84549-323_463cf19d-84cc-608e-e063-6294a90a07bc", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "84549-323", "generic_name": "LIDOCAINE HYDROCHLORIDE", "labeler_name": "ProPharma Distribution", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lidocaine Hydrochloride", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA040302", "marketing_category": "ANDA", "marketing_start_date": "20051209", "listing_expiration_date": "20261231"}