Package 51672-1395-0

{"route": ["TOPICAL"], "spl_id": "38ef2970-1212-d2fa-e063-6394a90a7570", "openfda": {"nui": ["N0000175607", "M0018962"], "unii": ["5688UTC01R"], "rxcui": ["198300"], "spl_set_id": ["9e964be5-8d67-46a8-888e-0351f9113f68"], "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 (51672-1395-0)  / 20 g in 1 TUBE", "package_ndc": "51672-1395-0", "marketing_start_date": "20190122"}, {"sample": false, "description": "1 TUBE in 1 CARTON (51672-1395-9)  / 45 g in 1 TUBE", "package_ndc": "51672-1395-9", "marketing_start_date": "20190122"}], "brand_name": "Tretinoin", "product_id": "51672-1395_38ef2970-1212-d2fa-e063-6394a90a7570", "dosage_form": "CREAM", "pharm_class": ["Retinoid [EPC]", "Retinoids [CS]"], "product_ndc": "51672-1395", "generic_name": "tretinoin", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tretinoin", "active_ingredients": [{"name": "TRETINOIN", "strength": "1 mg/g"}], "application_number": "ANDA211645", "marketing_category": "ANDA", "marketing_start_date": "20190122", "listing_expiration_date": "20261231"}