Package 0363-2101-08

Brand: jock itch

Generic: butenafine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0363-2101-08
Digits Only 0363210108
Product NDC 0363-2101
Description

1 TUBE in 1 CARTON (0363-2101-08) / 12 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2017-11-17
Brand jock itch
Generic butenafine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "39095706-5c7c-85d9-e063-6294a90a041f", "openfda": {"unii": ["R8XA2029ZI"], "rxcui": ["1298448"], "spl_set_id": ["6b13e8ad-b7dd-49e7-9469-3cac077c763e"], "manufacturer_name": ["Walgreen Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (0363-2101-08)  / 12 g in 1 TUBE", "package_ndc": "0363-2101-08", "marketing_start_date": "20171117"}], "brand_name": "Jock Itch", "product_id": "0363-2101_39095706-5c7c-85d9-e063-6294a90a041f", "dosage_form": "CREAM", "pharm_class": ["Benzylamine Antifungal [EPC]", "Benzylamines [CS]"], "product_ndc": "0363-2101", "generic_name": "Butenafine Hydrochloride", "labeler_name": "Walgreen Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Jock Itch", "active_ingredients": [{"name": "BUTENAFINE HYDROCHLORIDE", "strength": "10 mg/g"}], "application_number": "ANDA205181", "marketing_category": "ANDA", "marketing_start_date": "20171117", "listing_expiration_date": "20261231"}