Package 51991-526-01

Brand: terbinafine hydrochloride

Generic: terbinafine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51991-526-01
Digits Only 5199152601
Product NDC 51991-526
Product ID 51991-526_1603cd34-5cf4-4130-966f-c156d9237346
Description

100 TABLET in 1 BOTTLE (51991-526-01)

Marketing

Marketing Status
Marketed Since 2010-12-27
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": "1603cd34-5cf4-4130-966f-c156d9237346", "openfda": {"unii": ["012C11ZU6G"], "rxcui": ["313222"], "spl_set_id": ["c3832113-f517-4b4e-bf9c-31fce1a638e1"], "manufacturer_name": ["Breckenridge Pharmaceutical, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (51991-526-01)", "package_ndc": "51991-526-01", "marketing_start_date": "20101227"}], "brand_name": "Terbinafine Hydrochloride", "product_id": "51991-526_1603cd34-5cf4-4130-966f-c156d9237346", "dosage_form": "TABLET", "pharm_class": ["Allylamine Antifungal [EPC]", "Allylamine [CS]"], "product_ndc": "51991-526", "generic_name": "Terbinafine Hydrochloride", "labeler_name": "Breckenridge Pharmaceutical, 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"}