Package 59088-483-07

Brand: lidotran

Generic: lidocaine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 59088-483-07
Digits Only 5908848307
Product NDC 59088-483
Description

1 TUBE in 1 BAG (59088-483-07) / 85 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2022-09-19
Brand lidotran
Generic lidocaine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "cf715e54-c411-1e8f-e053-2995a90a076d", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1723991", "2611978"], "spl_set_id": ["cf715e54-c413-1e8f-e053-2995a90a076d"], "manufacturer_name": ["PureTek Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 BAG (59088-483-07)  / 85 g in 1 TUBE", "package_ndc": "59088-483-07", "marketing_start_date": "20220919"}], "brand_name": "Lidotran", "product_id": "59088-483_cf715e54-c411-1e8f-e053-2995a90a076d", "dosage_form": "CREAM", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "59088-483", "generic_name": "Lidocaine Hydrochloride", "labeler_name": "PureTek Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lidotran", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "38.8 mg/g"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20220919", "listing_expiration_date": "20261231"}