Package 51672-1368-2

{"route": ["TOPICAL"], "spl_id": "438dc98f-5e1f-b739-e063-6294a90a87a4", "openfda": {"unii": ["25UR9N9041"], "rxcui": ["1246096"], "spl_set_id": ["a740fc0d-45b3-411f-9dfd-f3d637b8a95f"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (51672-1368-2)  / 30 g in 1 TUBE", "package_ndc": "51672-1368-2", "marketing_start_date": "20160106"}, {"sample": false, "description": "1 TUBE in 1 CARTON (51672-1368-3)  / 60 g in 1 TUBE", "package_ndc": "51672-1368-3", "marketing_start_date": "20160106"}, {"sample": false, "description": "1 TUBE in 1 CARTON (51672-1368-6)  / 45 g in 1 TUBE", "package_ndc": "51672-1368-6", "marketing_start_date": "20160106"}], "brand_name": "Naftifine Hydrochloride", "product_id": "51672-1368_438dc98f-5e1f-b739-e063-6294a90a87a4", "dosage_form": "CREAM", "pharm_class": ["Allylamine Antifungal [EPC]", "Allylamine [CS]"], "product_ndc": "51672-1368", "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": "ANDA206901", "marketing_category": "ANDA", "marketing_start_date": "20160106", "listing_expiration_date": "20261231"}