lidocaine hydrochloride
Generic: lidocaine hydrochloride
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
lidocaine hydrochloride
Generic Name
lidocaine hydrochloride
Labeler
bryant ranch prepack
Dosage Form
SOLUTION
Routes
Active Ingredients
lidocaine hydrochloride anhydrous 40 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
63629-2096
Product ID
63629-2096_1ef3ae46-764c-4bc2-8eb2-7bd3691903a7
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA040710
Listing Expiration
2026-12-31
Marketing Start
2007-02-27
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
636292096
Hyphenated Format
63629-2096
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
ANDA040710 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 40 mg/mL
Packaging
- 50 mL in 1 BOTTLE (63629-2096-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1ef3ae46-764c-4bc2-8eb2-7bd3691903a7", "openfda": {"unii": ["EC2CNF7XFP"], "rxcui": ["1010878"], "spl_set_id": ["f581248d-697d-4174-aa42-afdf4ecce02e"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 BOTTLE (63629-2096-1)", "package_ndc": "63629-2096-1", "marketing_start_date": "20210211"}], "brand_name": "Lidocaine Hydrochloride", "product_id": "63629-2096_1ef3ae46-764c-4bc2-8eb2-7bd3691903a7", "dosage_form": "SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "63629-2096", "generic_name": "Lidocaine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lidocaine Hydrochloride", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE ANHYDROUS", "strength": "40 mg/mL"}], "application_number": "ANDA040710", "marketing_category": "ANDA", "marketing_start_date": "20070227", "listing_expiration_date": "20261231"}