Package 52000-441-02

Brand: 2.0% lidocaine burn

Generic: lidocaine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 52000-441-02
Digits Only 5200044102
Product NDC 52000-441
Description

59.1 mL in 1 BOTTLE, SPRAY (52000-441-02)

Marketing

Marketing Status
Marketed Since 2026-01-19
Brand 2.0% lidocaine burn
Generic lidocaine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "effa2131-872f-40a9-aa79-7e9197afe92e", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1010769"], "spl_set_id": ["e1911279-85f7-4053-b6da-8f4e991347a2"], "manufacturer_name": ["Universal Distribution Center LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "59.1 mL in 1 BOTTLE, SPRAY (52000-441-02)", "package_ndc": "52000-441-02", "marketing_start_date": "20260119"}], "brand_name": "2.0% LIDOCAINE BURN", "product_id": "52000-441_effa2131-872f-40a9-aa79-7e9197afe92e", "dosage_form": "SPRAY", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "52000-441", "generic_name": "Lidocaine Hydrochloride", "labeler_name": "Universal Distribution Center LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "2.0% LIDOCAINE BURN", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "2 g/100mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20260119", "listing_expiration_date": "20271231"}