Package 30142-210-02

Brand: butenafine hydrochloride athletes foot

Generic: butenafine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 30142-210-02
Digits Only 3014221002
Product NDC 30142-210
Description

1 TUBE in 1 CARTON (30142-210-02) / 30 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2021-03-21
Brand butenafine hydrochloride athletes foot
Generic butenafine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "39077171-1296-7988-e063-6394a90a0f13", "openfda": {"unii": ["R8XA2029ZI"], "rxcui": ["1298448"], "spl_set_id": ["2af91428-3fb9-4974-a55f-87aad750d05b"], "manufacturer_name": ["Kroger Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (30142-210-02)  / 30 g in 1 TUBE", "package_ndc": "30142-210-02", "marketing_start_date": "20210321"}], "brand_name": "Butenafine Hydrochloride Athletes Foot", "product_id": "30142-210_39077171-1296-7988-e063-6394a90a0f13", "dosage_form": "CREAM", "pharm_class": ["Benzylamine Antifungal [EPC]", "Benzylamines [CS]"], "product_ndc": "30142-210", "generic_name": "Butenafine Hydrochloride", "labeler_name": "Kroger Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Butenafine Hydrochloride", "brand_name_suffix": "Athletes Foot", "active_ingredients": [{"name": "BUTENAFINE HYDROCHLORIDE", "strength": "10 mg/g"}], "application_number": "ANDA205181", "marketing_category": "ANDA", "marketing_start_date": "20171116", "listing_expiration_date": "20261231"}