Package 50090-7300-1
Brand: terbinafine hydrochloride
Generic: terbinafine hydrochloridePackage Facts
Identity
Package NDC
50090-7300-1
Digits Only
5009073001
Product NDC
50090-7300
Description
90 TABLET in 1 BOTTLE (50090-7300-1)
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": "89a89899-6387-409a-b941-51a374183b43", "openfda": {"unii": ["012C11ZU6G"], "rxcui": ["313222"], "spl_set_id": ["8f6d7b1a-5a01-4cc5-b5b7-c126ae889557"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-7300-0)", "package_ndc": "50090-7300-0", "marketing_start_date": "20241014"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7300-1)", "package_ndc": "50090-7300-1", "marketing_start_date": "20241014"}], "brand_name": "terbinafine hydrochloride", "product_id": "50090-7300_89a89899-6387-409a-b941-51a374183b43", "dosage_form": "TABLET", "pharm_class": ["Allylamine Antifungal [EPC]", "Allylamine [CS]"], "product_ndc": "50090-7300", "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": "ANDA078163", "marketing_category": "ANDA", "marketing_start_date": "20220128", "listing_expiration_date": "20261231"}