Package 82804-220-42
Brand: terbinafine hydrochloride
Generic: terbinafine hydrochloridePackage Facts
Identity
Package NDC
82804-220-42
Digits Only
8280422042
Product NDC
82804-220
Description
42 TABLET in 1 BOTTLE, PLASTIC (82804-220-42)
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": "839cfff6-fb7f-489f-8cdb-5abda9bffd31", "openfda": {"upc": ["0382804220304"], "unii": ["012C11ZU6G"], "rxcui": ["313222"], "spl_set_id": ["53235270-6ffb-44c8-aa55-debf59e1d964"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (82804-220-30)", "package_ndc": "82804-220-30", "marketing_start_date": "20250424"}, {"sample": false, "description": "42 TABLET in 1 BOTTLE, PLASTIC (82804-220-42)", "package_ndc": "82804-220-42", "marketing_start_date": "20250904"}], "brand_name": "terbinafine hydrochloride", "product_id": "82804-220_839cfff6-fb7f-489f-8cdb-5abda9bffd31", "dosage_form": "TABLET", "pharm_class": ["Allylamine Antifungal [EPC]", "Allylamine [CS]"], "product_ndc": "82804-220", "generic_name": "terbinafine hydrochloride", "labeler_name": "Proficient Rx LP", "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"}