Package 63629-1993-1
Brand: terbinafine hydrochloride
Generic: terbinafine hydrochloridePackage Facts
Identity
Package NDC
63629-1993-1
Digits Only
6362919931
Product NDC
63629-1993
Description
100 TABLET in 1 BOTTLE (63629-1993-1)
Marketing
Marketing Status
Brand
terbinafine hydrochloride
Generic
terbinafine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2b858a61-405a-4352-9da9-978bb1f5a29a", "openfda": {"unii": ["012C11ZU6G"], "rxcui": ["313222"], "spl_set_id": ["facaea7f-cb4d-410f-85e4-e1ac9ff565ac"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (63629-1993-1)", "package_ndc": "63629-1993-1", "marketing_start_date": "20101227"}], "brand_name": "Terbinafine Hydrochloride", "product_id": "63629-1993_2b858a61-405a-4352-9da9-978bb1f5a29a", "dosage_form": "TABLET", "pharm_class": ["Allylamine Antifungal [EPC]", "Allylamine [CS]"], "product_ndc": "63629-1993", "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"}