Package 72162-2539-1

Brand: terbinafine

Generic: terbinafine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2539-1
Digits Only 7216225391
Product NDC 72162-2539
Description

100 TABLET in 1 BOTTLE (72162-2539-1)

Marketing

Marketing Status
Marketed Since 2025-09-18
Brand terbinafine
Generic terbinafine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8fd1e92a-7e29-4ed1-8c8e-dcd201bd53e9", "openfda": {"unii": ["012C11ZU6G"], "rxcui": ["313222"], "spl_set_id": ["838c6140-19b6-4c2b-aed7-3065bd67af07"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2539-1)", "package_ndc": "72162-2539-1", "marketing_start_date": "20250918"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (72162-2539-3)", "package_ndc": "72162-2539-3", "marketing_start_date": "20250918"}], "brand_name": "Terbinafine", "product_id": "72162-2539_8fd1e92a-7e29-4ed1-8c8e-dcd201bd53e9", "dosage_form": "TABLET", "pharm_class": ["Allylamine Antifungal [EPC]", "Allylamine [CS]"], "product_ndc": "72162-2539", "generic_name": "Terbinafine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Terbinafine", "active_ingredients": [{"name": "TERBINAFINE HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA078297", "marketing_category": "ANDA", "marketing_start_date": "20070702", "listing_expiration_date": "20261231"}