Package 50090-1048-0

Brand: terbinafine hydrochloride

Generic: terbinafine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-1048-0
Digits Only 5009010480
Product NDC 50090-1048
Product ID 50090-1048_1d9dab8d-1e3b-4c35-847d-57dbaa8c2ead
Description

30 TABLET in 1 BOTTLE (50090-1048-0)

Marketing

Marketing Status
Marketed Since 2014-11-28
Brand terbinafine hydrochloride
Generic terbinafine hydrochloride
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1d9dab8d-1e3b-4c35-847d-57dbaa8c2ead", "openfda": {"unii": ["012C11ZU6G"], "rxcui": ["313222"], "spl_set_id": ["6605103b-fd71-4438-8496-f48973b98901"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-1048-0)", "package_ndc": "50090-1048-0", "marketing_start_date": "20141128"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-1048-1)", "package_ndc": "50090-1048-1", "marketing_start_date": "20141128"}], "brand_name": "Terbinafine Hydrochloride", "product_id": "50090-1048_1d9dab8d-1e3b-4c35-847d-57dbaa8c2ead", "dosage_form": "TABLET", "pharm_class": ["Allylamine Antifungal [EPC]", "Allylamine [CS]"], "product_ndc": "50090-1048", "generic_name": "Terbinafine Hydrochloride", "labeler_name": "A-S Medication Solutions", "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"}