Package 84485-3605-4

Brand: lamisil at

Generic: terbinafine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 84485-3605-4
Digits Only 8448536054
Product NDC 84485-3605
Product ID 84485-3605_21f1bf77-4338-4b75-b513-80a0d98a722a
Description

120 g in 1 CAN (84485-3605-4)

Marketing

Marketing Status
Marketed Since 2025-12-10
Brand lamisil at
Generic terbinafine hydrochloride
Sample Package No

Linked Drug Pages (1)

Lamisil AT ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "21f1bf77-4338-4b75-b513-80a0d98a722a", "openfda": {"unii": ["012C11ZU6G"], "rxcui": ["992535", "992536"], "spl_set_id": ["21f1bf77-4338-4b75-b513-80a0d98a722a"], "manufacturer_name": ["Karo Healthcare Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 g in 1 CAN (84485-3605-4)", "package_ndc": "84485-3605-4", "marketing_start_date": "20251210"}], "brand_name": "Lamisil AT", "product_id": "84485-3605_21f1bf77-4338-4b75-b513-80a0d98a722a", "dosage_form": "SPRAY", "pharm_class": ["Allylamine Antifungal [EPC]", "Allylamine [CS]"], "product_ndc": "84485-3605", "generic_name": "terbinafine hydrochloride", "labeler_name": "Karo Healthcare Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Lamisil AT", "active_ingredients": [{"name": "TERBINAFINE HYDROCHLORIDE", "strength": "1 g/100g"}], "application_number": "NDA021124", "marketing_category": "NDA", "marketing_start_date": "20251210", "listing_expiration_date": "20261231"}