Package 82942-1001-1
Brand: burn
Generic: lidocaine hydrochloridePackage Facts
Identity
Package NDC
82942-1001-1
Digits Only
8294210011
Product NDC
82942-1001
Description
.9 g in 1 PACKET (82942-1001-1)
Marketing
Marketing Status
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": "369d70f9-9b65-e8f2-e063-6294a90a6b86", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1011852"], "spl_set_id": ["d4b09055-b93e-466f-9e24-cae098af6e24"], "manufacturer_name": ["J&A Digital Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": ".9 g in 1 PACKET (82942-1001-1)", "package_ndc": "82942-1001-1", "marketing_start_date": "20221001"}], "brand_name": "Burn", "product_id": "82942-1001_369d70f9-9b65-e8f2-e063-6294a90a6b86", "dosage_form": "GEL", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "82942-1001", "generic_name": "LIDOCAINE HYDROCHLORIDE", "labeler_name": "J&A Digital Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Burn", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "20 mg/g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20221001", "listing_expiration_date": "20261231"}