Package 59088-307-07

Brand: lidotral 3.88% roll on

Generic: lidocaine hci
NDC Package

Package Facts

Identity

Package NDC 59088-307-07
Digits Only 5908830707
Product NDC 59088-307
Description

85 g in 1 BOTTLE (59088-307-07)

Marketing

Marketing Status
Marketed Since 2024-02-28
Brand lidotral 3.88% roll on
Generic lidocaine hci
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "db1085fe-0a1e-c4cc-e053-2a95a90aa838", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["2675768", "2675772"], "spl_set_id": ["db1085fe-0a1f-c4cc-e053-2a95a90aa838"], "manufacturer_name": ["PureTek Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "85 g in 1 BOTTLE (59088-307-07)", "package_ndc": "59088-307-07", "marketing_start_date": "20240228"}], "brand_name": "Lidotral 3.88% Roll on", "product_id": "59088-307_db1085fe-0a1e-c4cc-e053-2a95a90aa838", "dosage_form": "GEL", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "59088-307", "generic_name": "Lidocaine HCI", "labeler_name": "PureTek Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lidotral 3.88% Roll on", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "38.8 mg/g"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20240228", "listing_expiration_date": "20261231"}