Package 68071-4500-1

Brand: terbinafine hydrochloride

Generic: terbinafine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-4500-1
Digits Only 6807145001
Product NDC 68071-4500
Product ID 68071-4500_1a8daeb9-2c25-ccc0-e063-6394a90a9cae
Description

100 TABLET in 1 BOTTLE (68071-4500-1)

Marketing

Marketing Status
Marketed Since 2018-07-19
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": "1a8daeb9-2c25-ccc0-e063-6394a90a9cae", "openfda": {"upc": ["0368071450019"], "unii": ["012C11ZU6G"], "rxcui": ["313222"], "spl_set_id": ["715cae3e-4e86-48b3-e053-2a95a90afdc2"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68071-4500-1)", "package_ndc": "68071-4500-1", "marketing_start_date": "20180719"}], "brand_name": "Terbinafine Hydrochloride", "product_id": "68071-4500_1a8daeb9-2c25-ccc0-e063-6394a90a9cae", "dosage_form": "TABLET", "pharm_class": ["Allylamine Antifungal [EPC]", "Allylamine [CS]"], "product_ndc": "68071-4500", "generic_name": "Terbinafine Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "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"}