Package 79481-0086-1

Brand: butenafine hydrochloride

Generic: butenafine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 79481-0086-1
Digits Only 7948100861
Product NDC 79481-0086
Description

1 TUBE in 1 CARTON (79481-0086-1) / 30 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2023-11-30
Brand butenafine hydrochloride
Generic butenafine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "39070e62-eb92-10ca-e063-6394a90a7564", "openfda": {"unii": ["R8XA2029ZI"], "rxcui": ["1298448"], "spl_set_id": ["4e88068b-1449-43b4-9c7c-4ad8e877459b"], "manufacturer_name": ["MEIJER DISTRIBUTION INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (79481-0086-1)  / 30 g in 1 TUBE", "package_ndc": "79481-0086-1", "marketing_start_date": "20231130"}], "brand_name": "Butenafine Hydrochloride", "product_id": "79481-0086_39070e62-eb92-10ca-e063-6394a90a7564", "dosage_form": "CREAM", "pharm_class": ["Benzylamine Antifungal [EPC]", "Benzylamines [CS]"], "product_ndc": "79481-0086", "generic_name": "Butenafine Hydrochloride", "labeler_name": "MEIJER DISTRIBUTION INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Butenafine Hydrochloride", "active_ingredients": [{"name": "BUTENAFINE HYDROCHLORIDE", "strength": "10 mg/g"}], "application_number": "ANDA205181", "marketing_category": "ANDA", "marketing_start_date": "20231130", "listing_expiration_date": "20261231"}