Package 69842-989-08

Brand: butenafine hydrochloride 1%

Generic: butenafine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 69842-989-08
Digits Only 6984298908
Product NDC 69842-989
Description

1 TUBE in 1 CARTON (69842-989-08) / 12 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2018-10-18
Brand butenafine hydrochloride 1%
Generic butenafine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "39077171-1285-7988-e063-6394a90a0f13", "openfda": {"unii": ["R8XA2029ZI"], "rxcui": ["1298448"], "spl_set_id": ["83830b24-bc94-4764-a6ca-3193abd9de66"], "manufacturer_name": ["CVS Pharmacy"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (69842-989-08)  / 12 g in 1 TUBE", "package_ndc": "69842-989-08", "marketing_start_date": "20181018"}], "brand_name": "Butenafine Hydrochloride 1%", "product_id": "69842-989_39077171-1285-7988-e063-6394a90a0f13", "dosage_form": "CREAM", "pharm_class": ["Benzylamine Antifungal [EPC]", "Benzylamines [CS]"], "product_ndc": "69842-989", "generic_name": "Butenafine Hydrochloride", "labeler_name": "CVS Pharmacy", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Butenafine Hydrochloride 1%", "active_ingredients": [{"name": "BUTENAFINE HYDROCHLORIDE", "strength": "10 mg/g"}], "application_number": "ANDA205181", "marketing_category": "ANDA", "marketing_start_date": "20181018", "listing_expiration_date": "20261231"}