Package 84485-3748-3

Brand: lamisil at cream

Generic: terbinafine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 84485-3748-3
Digits Only 8448537483
Product NDC 84485-3748
Description

1 TUBE in 1 CARTON (84485-3748-3) / 30 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2024-11-01
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": "58726dc3-45ee-4543-8863-3949940fb64e", "openfda": {"unii": ["012C11ZU6G"], "rxcui": ["992528", "992530"], "spl_set_id": ["7f8434c2-60c9-4aeb-b0b8-f69107e74609"], "manufacturer_name": ["Karo Healthcare Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (84485-3748-3)  / 30 g in 1 TUBE", "package_ndc": "84485-3748-3", "marketing_start_date": "20241101"}], "brand_name": "Lamisil AT Cream", "product_id": "84485-3748_58726dc3-45ee-4543-8863-3949940fb64e", "dosage_form": "CREAM", "pharm_class": ["Allylamine Antifungal [EPC]", "Allylamine [CS]"], "product_ndc": "84485-3748", "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": "20241101", "listing_expiration_date": "20261231"}