Package 21130-965-01

Brand: butenafine hydrochloride

Generic: butenafine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 21130-965-01
Digits Only 2113096501
Product NDC 21130-965
Product ID 21130-965_3907a168-2eff-5817-e063-6394a90a2f83
Description

1 TUBE in 1 CARTON (21130-965-01) / 30 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2023-04-19
Brand butenafine hydrochloride
Generic butenafine hydrochloride
Sample Package No

Linked Drug Pages (1)

Butenafine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "3907a168-2eff-5817-e063-6394a90a2f83", "openfda": {"unii": ["R8XA2029ZI"], "rxcui": ["1298448"], "spl_set_id": ["098dee89-0f7b-4341-a691-bfe6077ff353"], "manufacturer_name": ["Albertsons"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (21130-965-01)  / 30 g in 1 TUBE", "package_ndc": "21130-965-01", "marketing_start_date": "20230419"}], "brand_name": "Butenafine Hydrochloride", "product_id": "21130-965_3907a168-2eff-5817-e063-6394a90a2f83", "dosage_form": "CREAM", "pharm_class": ["Benzylamine Antifungal [EPC]", "Benzylamines [CS]"], "product_ndc": "21130-965", "generic_name": "Butenafine Hydrochloride", "labeler_name": "Albertsons", "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": "20230419", "listing_expiration_date": "20261231"}