Package 73598-0671-1

Brand: burn

Generic: lidocaine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 73598-0671-1
Digits Only 7359806711
Product NDC 73598-0671
Description

59.1 mL in 1 BOTTLE, SPRAY (73598-0671-1)

Marketing

Marketing Status
Marketed Since 2020-02-14
Brand burn
Generic lidocaine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "175d06c4-4ca4-4036-a6ff-2a4148f31ab9", "openfda": {"upc": ["0747200606716"], "unii": ["V13007Z41A"], "rxcui": ["1010769"], "spl_set_id": ["5a4ac4cc-015a-48e7-81f8-93a895049afd"], "manufacturer_name": ["JHK Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "59.1 mL in 1 BOTTLE, SPRAY (73598-0671-1)", "package_ndc": "73598-0671-1", "marketing_start_date": "20200214"}], "brand_name": "Burn", "product_id": "73598-0671_175d06c4-4ca4-4036-a6ff-2a4148f31ab9", "dosage_form": "SPRAY", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "73598-0671", "generic_name": "lidocaine hydrochloride", "labeler_name": "JHK Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Burn", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200214", "listing_expiration_date": "20261231"}