Package 59088-304-03

Brand: lidotral two percent

Generic: lidocaine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 59088-304-03
Digits Only 5908830403
Product NDC 59088-304
Description

30 mL in 1 BOTTLE, SPRAY (59088-304-03)

Marketing

Marketing Status
Marketed Since 2024-05-14
Brand lidotral two percent
Generic lidocaine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "185d3e09-4006-b032-e063-6294a90a5efe", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1010769"], "spl_set_id": ["185d3e09-4005-b032-e063-6294a90a5efe"], "manufacturer_name": ["PureTek Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 mL in 1 BOTTLE, SPRAY (59088-304-03)", "package_ndc": "59088-304-03", "marketing_start_date": "20240514"}], "brand_name": "Lidotral Two Percent", "product_id": "59088-304_185d3e09-4006-b032-e063-6294a90a5efe", "dosage_form": "SPRAY", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "59088-304", "generic_name": "Lidocaine Hydrochloride", "labeler_name": "PureTek Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lidotral Two Percent", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "20 mg/mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20240514", "listing_expiration_date": "20261231"}