Package 11673-436-01

Brand: jock itch cream

Generic: butenafine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 11673-436-01
Digits Only 1167343601
Product NDC 11673-436
Product ID 11673-436_3909394c-0658-e681-e063-6394a90a5e04
Description

1 TUBE in 1 CARTON (11673-436-01) / 12 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2024-11-15
Brand jock itch cream
Generic butenafine hydrochloride
Sample Package No

Linked Drug Pages (1)

Jock Itch Cream ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "3909394c-0658-e681-e063-6394a90a5e04", "openfda": {"upc": ["0311673436011"], "unii": ["R8XA2029ZI"], "rxcui": ["1298448"], "spl_set_id": ["1d8a17ae-4e25-f591-e063-6394a90a35dd"], "manufacturer_name": ["TARGET CORPORATION"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (11673-436-01)  / 12 g in 1 TUBE", "package_ndc": "11673-436-01", "marketing_start_date": "20241115"}], "brand_name": "Jock Itch Cream", "product_id": "11673-436_3909394c-0658-e681-e063-6394a90a5e04", "dosage_form": "CREAM", "pharm_class": ["Benzylamine Antifungal [EPC]", "Benzylamines [CS]"], "product_ndc": "11673-436", "generic_name": "Butenafine Hydrochloride", "labeler_name": "TARGET CORPORATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Jock Itch Cream", "active_ingredients": [{"name": "BUTENAFINE HYDROCHLORIDE", "strength": "10 mg/g"}], "application_number": "ANDA205181", "marketing_category": "ANDA", "marketing_start_date": "20241115", "listing_expiration_date": "20261231"}