Package 16714-795-01

Brand: terbinafine

Generic: terbinafine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 16714-795-01
Digits Only 1671479501
Product NDC 16714-795
Product ID 16714-795_959f3136-b10d-4a73-a11a-1fae5bd72fb6
Description

30 TABLET in 1 BOTTLE (16714-795-01)

Marketing

Marketing Status
Marketed Since 2007-07-02
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": "959f3136-b10d-4a73-a11a-1fae5bd72fb6", "openfda": {"unii": ["012C11ZU6G"], "rxcui": ["313222"], "spl_set_id": ["8f87e3e1-4c9c-497a-af20-8ab52cfeef60"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (16714-795-01)", "package_ndc": "16714-795-01", "marketing_start_date": "20070702"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (16714-795-02)", "package_ndc": "16714-795-02", "marketing_start_date": "20070702"}], "brand_name": "Terbinafine", "product_id": "16714-795_959f3136-b10d-4a73-a11a-1fae5bd72fb6", "dosage_form": "TABLET", "pharm_class": ["Allylamine Antifungal [EPC]", "Allylamine [CS]"], "product_ndc": "16714-795", "generic_name": "Terbinafine Hydrochloride", "labeler_name": "NorthStar Rx LLC", "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"}