lidocaine hydrochloride
Generic: lidocaine hydrochloride
Labeler: chartwell rx, llcDrug Facts
Product Profile
Brand Name
lidocaine hydrochloride
Generic Name
lidocaine hydrochloride
Labeler
chartwell rx, llc
Dosage Form
SOLUTION
Routes
Active Ingredients
lidocaine hydrochloride anhydrous 20 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
62135-712
Product ID
62135-712_4936d399-9101-8558-e063-6294a90a639c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA040708
Listing Expiration
2027-12-31
Marketing Start
2007-02-27
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
62135712
Hyphenated Format
62135-712
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
ANDA040708 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/mL
Packaging
- 100 mL in 1 BOTTLE (62135-712-42)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["OROPHARYNGEAL"], "spl_id": "4936d399-9101-8558-e063-6294a90a639c", "openfda": {"upc": ["0362135712426"], "unii": ["EC2CNF7XFP"], "rxcui": ["1010739"], "spl_set_id": ["c05f49a2-7512-48e7-9730-f8ee05519b9d"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (62135-712-42)", "package_ndc": "62135-712-42", "marketing_start_date": "20230616"}], "brand_name": "Lidocaine Hydrochloride", "product_id": "62135-712_4936d399-9101-8558-e063-6294a90a639c", "dosage_form": "SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "62135-712", "generic_name": "Lidocaine Hydrochloride", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lidocaine Hydrochloride", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE ANHYDROUS", "strength": "20 mg/mL"}], "application_number": "ANDA040708", "marketing_category": "ANDA", "marketing_start_date": "20070227", "listing_expiration_date": "20271231"}