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
84549-277
Product ID
84549-277_463e3815-f8c9-449a-e063-6394a90a6aa6
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA088327
Listing Expiration
2026-12-31
Marketing Start
2005-06-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
84549277
Hyphenated Format
84549-277
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
ANDA088327 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/mL
Packaging
- 50 mL in 1 VIAL, MULTI-DOSE (84549-277-02)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INFILTRATION", "PERINEURAL"], "spl_id": "463e3815-f8c9-449a-e063-6394a90a6aa6", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1010671"], "spl_set_id": ["42d9e4cf-ca73-ec6d-e063-6394a90ae937"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 VIAL, MULTI-DOSE (84549-277-02)", "package_ndc": "84549-277-02", "marketing_start_date": "20251010"}], "brand_name": "Lidocaine Hydrochloride", "product_id": "84549-277_463e3815-f8c9-449a-e063-6394a90a6aa6", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "84549-277", "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": "ANDA088327", "marketing_category": "ANDA", "marketing_start_date": "20050615", "listing_expiration_date": "20261231"}