Package 50090-7300-1

Brand: terbinafine hydrochloride

Generic: terbinafine hydrochloride
NDC Package

Package 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
Marketed Since 2024-10-14
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"}