Package 51672-1407-0

{"route": ["TOPICAL"], "spl_id": "3629e80a-923f-b80a-e063-6394a90a44d3", "openfda": {"nui": ["N0000175607", "M0018962"], "unii": ["5688UTC01R"], "rxcui": ["106302"], "spl_set_id": ["2a31b13b-5cc8-4f6a-b364-872f6a478025"], "pharm_class_cs": ["Retinoids [CS]"], "pharm_class_epc": ["Retinoid [EPC]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (51672-1407-0)  / 20 g in 1 TUBE", "package_ndc": "51672-1407-0", "marketing_start_date": "20230105"}, {"sample": false, "description": "1 TUBE in 1 CARTON (51672-1407-9)  / 45 g in 1 TUBE", "package_ndc": "51672-1407-9", "marketing_start_date": "20230105"}], "brand_name": "Tretinoin", "product_id": "51672-1407_3629e80a-923f-b80a-e063-6394a90a44d3", "dosage_form": "CREAM", "pharm_class": ["Retinoid [EPC]", "Retinoids [CS]"], "product_ndc": "51672-1407", "generic_name": "tretinoin", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tretinoin", "active_ingredients": [{"name": "TRETINOIN", "strength": ".25 mg/g"}], "application_number": "ANDA215713", "marketing_category": "ANDA", "marketing_start_date": "20230105", "listing_expiration_date": "20261231"}