lidocaine hydrochloride

Generic: lidocaine hydrochloride

Labeler: lannett company, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lidocaine hydrochloride
Generic Name lidocaine hydrochloride
Labeler lannett company, inc.
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

lidocaine hydrochloride anhydrous 40 mg/mL

Manufacturer
Lannett Company, Inc.

Identifiers & Regulatory

Product NDC 0527-6004
Product ID 0527-6004_94508c6a-c451-46de-850c-a63f5152df01
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040710
Listing Expiration 2026-12-31
Marketing Start 2007-02-27

Pharmacologic Class

Classes
amide local anesthetic [epc] amides [cs] antiarrhythmic [epc] local anesthesia [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 05276004
Hyphenated Format 0527-6004

Supplemental Identifiers

RxCUI
1010878
UPC
0305276004807
UNII
EC2CNF7XFP

Packaging Origin

Original Packager
true

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (0527-6004-80) / 50 mL in 1 BOTTLE
source: ndc

Packages (1)

Ingredients (1)

lidocaine hydrochloride anhydrous (40 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "94508c6a-c451-46de-850c-a63f5152df01", "openfda": {"upc": ["0305276004807"], "unii": ["EC2CNF7XFP"], "rxcui": ["1010878"], "spl_set_id": ["c3353e08-2a8c-4ace-ba89-114f7131b8de"], "manufacturer_name": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0527-6004-80)  / 50 mL in 1 BOTTLE", "package_ndc": "0527-6004-80", "marketing_start_date": "20070227"}], "brand_name": "Lidocaine Hydrochloride", "product_id": "0527-6004_94508c6a-c451-46de-850c-a63f5152df01", "dosage_form": "SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "0527-6004", "generic_name": "Lidocaine Hydrochloride", "labeler_name": "Lannett Company, Inc.", "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"}