Package 59088-233-05
Brand: bruselix gel
Generic: lidocaine hci 3.88%Package Facts
Identity
Package NDC
59088-233-05
Digits Only
5908823305
Product NDC
59088-233
Description
57 g in 1 TUBE (59088-233-05)
Marketing
Marketing Status
Brand
bruselix gel
Generic
lidocaine hci 3.88%
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "155d0c2a-6027-c589-e063-6394a90a07dd", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["2675768", "2678305"], "spl_set_id": ["1420ec27-64f3-9117-e063-6294a90a8ece"], "manufacturer_name": ["PureTek Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "57 g in 1 TUBE (59088-233-05)", "package_ndc": "59088-233-05", "marketing_start_date": "20240321"}], "brand_name": "Bruselix Gel", "product_id": "59088-233_155d0c2a-6027-c589-e063-6394a90a07dd", "dosage_form": "GEL", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "59088-233", "generic_name": "Lidocaine HCI 3.88%", "labeler_name": "PureTek Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bruselix Gel", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "38.8 mg/g"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20240321", "listing_expiration_date": "20261231"}