Package 51672-1376-6

{"route": ["TOPICAL"], "spl_id": "4aa35016-7749-87c7-e063-6394a90ac5c6", "openfda": {"unii": ["25UR9N9041"], "rxcui": ["1433734"], "spl_set_id": ["92d3ec30-2176-49cd-8a70-668ef65e7663"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (51672-1376-3)  / 60 g in 1 TUBE", "package_ndc": "51672-1376-3", "marketing_start_date": "20230401"}, {"sample": false, "description": "1 TUBE in 1 CARTON (51672-1376-6)  / 45 g in 1 TUBE", "package_ndc": "51672-1376-6", "marketing_start_date": "20230401"}], "brand_name": "Naftifine Hydrochloride", "product_id": "51672-1376_4aa35016-7749-87c7-e063-6394a90ac5c6", "dosage_form": "GEL", "pharm_class": ["Allylamine Antifungal [EPC]", "Allylamine [CS]"], "product_ndc": "51672-1376", "generic_name": "Naftifine Hydrochloride", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naftifine Hydrochloride", "active_ingredients": [{"name": "NAFTIFINE HYDROCHLORIDE", "strength": "20 mg/g"}], "application_number": "ANDA208201", "marketing_category": "ANDA", "marketing_start_date": "20230401", "listing_expiration_date": "20271231"}