Package 51672-1370-1

{"route": ["TOPICAL"], "spl_id": "390bed79-7314-fbe9-e063-6394a90ae7f1", "openfda": {"unii": ["RG38I2P540"], "rxcui": ["311877"], "spl_set_id": ["6719ffba-3430-4fa9-b65b-c5c195ee1b35"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (51672-1370-1)  / 15 g in 1 TUBE", "package_ndc": "51672-1370-1", "marketing_start_date": "20200427"}, {"sample": false, "description": "1 TUBE in 1 CARTON (51672-1370-2)  / 30 g in 1 TUBE", "package_ndc": "51672-1370-2", "marketing_start_date": "20200427"}], "brand_name": "Mupirocin", "product_id": "51672-1370_390bed79-7314-fbe9-e063-6394a90ae7f1", "dosage_form": "CREAM", "pharm_class": ["RNA Synthetase Inhibitor Antibacterial [EPC]", "RNA Synthetase Inhibitors [MoA]"], "product_ndc": "51672-1370", "generic_name": "Mupirocin Calcium", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mupirocin", "active_ingredients": [{"name": "MUPIROCIN CALCIUM", "strength": "20 mg/g"}], "application_number": "ANDA207116", "marketing_category": "ANDA", "marketing_start_date": "20200427", "listing_expiration_date": "20261231"}