Package 84485-3607-1

Brand: lamisil at cream

Generic: terbinafine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 84485-3607-1
Digits Only 8448536071
Product NDC 84485-3607
Description

1 TUBE in 1 CARTON (84485-3607-1) / 12 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2025-01-20
Brand lamisil at cream
Generic terbinafine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "dc1dfa6d-7d6d-43cf-a25a-8497e3430bcd", "openfda": {"unii": ["012C11ZU6G"], "rxcui": ["992528", "992530"], "spl_set_id": ["0f59271d-997f-4dcc-aae3-900b53df1c95"], "manufacturer_name": ["Karo Healthcare Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (84485-3607-1)  / 12 g in 1 TUBE", "package_ndc": "84485-3607-1", "marketing_start_date": "20250120"}], "brand_name": "Lamisil AT Cream", "product_id": "84485-3607_dc1dfa6d-7d6d-43cf-a25a-8497e3430bcd", "dosage_form": "CREAM", "pharm_class": ["Allylamine Antifungal [EPC]", "Allylamine [CS]"], "product_ndc": "84485-3607", "generic_name": "Terbinafine Hydrochloride", "labeler_name": "Karo Healthcare Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Lamisil AT Cream", "active_ingredients": [{"name": "TERBINAFINE HYDROCHLORIDE", "strength": "1 g/100g"}], "application_number": "NDA020980", "marketing_category": "NDA", "marketing_start_date": "20250120", "listing_expiration_date": "20261231"}