lidocaine hydrochloride
Generic: lidocaine hydrochloride
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
lidocaine hydrochloride
Generic Name
lidocaine hydrochloride
Labeler
remedyrepack inc.
Dosage Form
INJECTION
Routes
Active Ingredients
lidocaine hydrochloride 20 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
70518-4176
Product ID
70518-4176_3fba1106-c179-3e9e-e063-6394a90a1cff
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA083173
Listing Expiration
2026-12-31
Marketing Start
2024-09-18
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705184176
Hyphenated Format
70518-4176
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
ANDA083173 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/mL
Packaging
- 10 SYRINGE in 1 PACKAGE (70518-4176-0) / 5 mL in 1 SYRINGE (70518-4176-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "3fba1106-c179-3e9e-e063-6394a90a1cff", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1012068"], "spl_set_id": ["f824b48c-7039-4ce1-b3df-b3597aba5beb"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "10 SYRINGE in 1 PACKAGE (70518-4176-0) / 5 mL in 1 SYRINGE (70518-4176-1)", "package_ndc": "70518-4176-0", "marketing_start_date": "20240918"}], "brand_name": "Lidocaine Hydrochloride", "product_id": "70518-4176_3fba1106-c179-3e9e-e063-6394a90a1cff", "dosage_form": "INJECTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "70518-4176", "generic_name": "Lidocaine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lidocaine Hydrochloride", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA083173", "marketing_category": "ANDA", "marketing_start_date": "20240918", "listing_expiration_date": "20261231"}