Package 11523-0082-1
Brand: lotrimin ultra
Generic: butenafine hydrochloridePackage Facts
Identity
Package NDC
11523-0082-1
Digits Only
1152300821
Product NDC
11523-0082
Description
1 TUBE, WITH APPLICATOR in 1 CARTON (11523-0082-1) / 20 g in 1 TUBE, WITH APPLICATOR
Marketing
Marketing Status
Brand
lotrimin ultra
Generic
butenafine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4526ca36-993f-b574-e063-6294a90a8fba", "openfda": {"upc": ["0000000000000"], "unii": ["R8XA2029ZI"], "rxcui": ["1298448"], "spl_set_id": ["d11dfdf6-9b36-03bc-e053-2995a90a0bc3"], "manufacturer_name": ["Bayer Healthcare LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE, WITH APPLICATOR in 1 CARTON (11523-0082-1) / 20 g in 1 TUBE, WITH APPLICATOR", "package_ndc": "11523-0082-1", "marketing_start_date": "20211220"}], "brand_name": "Lotrimin Ultra", "product_id": "11523-0082_4526ca36-993f-b574-e063-6294a90a8fba", "dosage_form": "CREAM", "pharm_class": ["Benzylamine Antifungal [EPC]", "Benzylamines [CS]"], "product_ndc": "11523-0082", "generic_name": "Butenafine hydrochloride", "labeler_name": "Bayer Healthcare LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Lotrimin Ultra", "active_ingredients": [{"name": "BUTENAFINE HYDROCHLORIDE", "strength": "1 g/100g"}], "application_number": "NDA021307", "marketing_category": "NDA", "marketing_start_date": "20211220", "listing_expiration_date": "20261231"}