Package 72162-1595-1

Brand: terbinafine hydrochloride

Generic: terbinafine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1595-1
Digits Only 7216215951
Product NDC 72162-1595
Product ID 72162-1595_f9f34f4d-d49d-4921-9e3e-8b6e2fd16d9f
Description

100 TABLET in 1 BOTTLE (72162-1595-1)

Marketing

Marketing Status
Marketed Since 2024-02-07
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": ["ORAL"], "spl_id": "f9f34f4d-d49d-4921-9e3e-8b6e2fd16d9f", "openfda": {"unii": ["012C11ZU6G"], "rxcui": ["313222"], "spl_set_id": ["e2ecf7a5-1c84-4977-8a87-d1bfb9658668"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-1595-1)", "package_ndc": "72162-1595-1", "marketing_start_date": "20240207"}], "brand_name": "Terbinafine Hydrochloride", "product_id": "72162-1595_f9f34f4d-d49d-4921-9e3e-8b6e2fd16d9f", "dosage_form": "TABLET", "pharm_class": ["Allylamine Antifungal [EPC]", "Allylamine [CS]"], "product_ndc": "72162-1595", "generic_name": "Terbinafine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Terbinafine Hydrochloride", "active_ingredients": [{"name": "TERBINAFINE HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA077714", "marketing_category": "ANDA", "marketing_start_date": "20101227", "listing_expiration_date": "20261231"}