Package 80684-098-00

Brand: thera plus max strength lidocaine pain relief liquid

Generic: lidocaine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 80684-098-00
Digits Only 8068409800
Product NDC 80684-098
Description

74 mL in 1 BOTTLE (80684-098-00)

Marketing

Marketing Status
Marketed Since 2024-02-01
Brand thera plus max strength lidocaine pain relief liquid
Generic lidocaine hydrochloride
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "0b61e01d-3530-d2a1-e063-6294a90a513c", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1987647"], "spl_set_id": ["0a228b06-0e1c-6c75-e063-6294a90a9a0e"], "manufacturer_name": ["Fourstar Group USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "74 mL in 1 BOTTLE (80684-098-00)", "package_ndc": "80684-098-00", "marketing_start_date": "20240201"}], "brand_name": "Thera Plus Max Strength Lidocaine Pain Relief Liquid", "product_id": "80684-098_0b61e01d-3530-d2a1-e063-6294a90a513c", "dosage_form": "LIQUID", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "80684-098", "generic_name": "LIDOCAINE HYDROCHLORIDE", "labeler_name": "Fourstar Group USA, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Thera Plus Max Strength Lidocaine Pain Relief Liquid", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "40 mg/mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240201", "listing_expiration_date": "20261231"}