Package 59088-327-07

Brand: lidotral 5 percent roll on gel

Generic: lidocaine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 59088-327-07
Digits Only 5908832707
Product NDC 59088-327
Description

85 g in 1 BOTTLE, WITH APPLICATOR (59088-327-07)

Marketing

Marketing Status
Marketed Since 2024-08-02
Brand lidotral 5 percent roll on gel
Generic lidocaine hydrochloride
Sample Package No

Linked Drug Pages (2)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "1c4c9ce5-f12d-9c47-e063-6294a90a0b3c", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1010057"], "spl_set_id": ["1c4c9ce5-f12d-9c47-e063-6294a90a0b3c"], "manufacturer_name": ["Puretek Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "85 g in 1 BOTTLE, WITH APPLICATOR (59088-327-07)", "package_ndc": "59088-327-07", "marketing_start_date": "20240802"}], "brand_name": "Lidotral 5 Percent Roll On Gel", "product_id": "59088-327_1c4c9ce5-f12d-9c47-e063-6294a90a0b3c", "dosage_form": "GEL", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "59088-327", "generic_name": "Lidocaine Hydrochloride", "labeler_name": "Puretek Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lidotral 5 Percent Roll On Gel", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "50 mg/g"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20240802", "listing_expiration_date": "20261231"}