Package 71205-061-30

Brand: terbinafine

Generic: terbinafine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71205-061-30
Digits Only 7120506130
Product NDC 71205-061
Product ID 71205-061_f2548203-c59d-46a1-bf6f-098e91344380
Description

30 TABLET in 1 BOTTLE (71205-061-30)

Marketing

Marketing Status
Marketed Since 2018-07-02
Brand terbinafine
Generic terbinafine hydrochloride
Sample Package No

Linked Drug Pages (1)

Terbinafine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f2548203-c59d-46a1-bf6f-098e91344380", "openfda": {"upc": ["0371205061302"], "unii": ["012C11ZU6G"], "rxcui": ["313222"], "spl_set_id": ["0a54cc4f-0789-46ce-875f-df759aa95d9c"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-061-30)", "package_ndc": "71205-061-30", "marketing_start_date": "20180702"}], "brand_name": "Terbinafine", "product_id": "71205-061_f2548203-c59d-46a1-bf6f-098e91344380", "dosage_form": "TABLET", "pharm_class": ["Allylamine Antifungal [EPC]", "Allylamine [CS]"], "product_ndc": "71205-061", "generic_name": "Terbinafine Hydrochloride", "labeler_name": "Proficient Rx LP", "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"}