Package 84269-3500-1

Brand: lidocaine hydrochloride

Generic: lidocaine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 84269-3500-1
Digits Only 8426935001
Product NDC 84269-3500
Description

59.1 mL in 1 BOTTLE, SPRAY (84269-3500-1)

Marketing

Marketing Status
Marketed Since 2024-09-01
Brand lidocaine hydrochloride
Generic lidocaine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "1fd1b3b8-0ac5-d0ad-e063-6394a90a72da", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1010769"], "spl_set_id": ["1fd1a4b3-b6fd-0d4c-e063-6394a90a3680"], "manufacturer_name": ["Wildman Business Group"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "59.1 mL in 1 BOTTLE, SPRAY (84269-3500-1)", "package_ndc": "84269-3500-1", "marketing_start_date": "20240901"}], "brand_name": "Lidocaine Hydrochloride", "product_id": "84269-3500_1fd1b3b8-0ac5-d0ad-e063-6394a90a72da", "dosage_form": "LIQUID", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "84269-3500", "generic_name": "Lidocaine Hydrochloride", "labeler_name": "Wildman Business Group", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Lidocaine Hydrochloride", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240901", "listing_expiration_date": "20261231"}