Package 73469-7215-2

Brand: terbinafine hydrochloride

Generic: terbinafine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 73469-7215-2
Digits Only 7346972152
Product NDC 73469-7215
Product ID 73469-7215_3e8bf437-1d46-8e1d-e063-6294a90a15e9
Description

1 TUBE in 1 CARTON (73469-7215-2) / 30 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2025-09-11
Brand terbinafine hydrochloride
Generic terbinafine hydrochloride
Sample Package No

Linked Drug Pages (1)

Terbinafine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "3e8bf437-1d46-8e1d-e063-6294a90a15e9", "openfda": {"unii": ["012C11ZU6G"], "rxcui": ["992528"], "spl_set_id": ["31f59302-eaee-211b-e063-6294a90a08b0"], "manufacturer_name": ["Scholl's Wellness Company LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (73469-7215-2)  / 30 g in 1 TUBE", "package_ndc": "73469-7215-2", "marketing_start_date": "20250911"}], "brand_name": "Terbinafine Hydrochloride", "product_id": "73469-7215_3e8bf437-1d46-8e1d-e063-6294a90a15e9", "dosage_form": "CREAM", "pharm_class": ["Allylamine Antifungal [EPC]", "Allylamine [CS]"], "product_ndc": "73469-7215", "generic_name": "Terbinafine Hydrochloride", "labeler_name": "Scholl's Wellness Company LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Terbinafine Hydrochloride", "active_ingredients": [{"name": "TERBINAFINE HYDROCHLORIDE", "strength": "1 g/100g"}], "application_number": "ANDA077511", "marketing_category": "ANDA", "marketing_start_date": "20250911", "listing_expiration_date": "20261231"}