Package 51672-1394-9

{"route": ["TOPICAL"], "spl_id": "38ef297e-e4cb-0593-e063-6294a90a324d", "openfda": {"nui": ["N0000175607", "M0018962"], "unii": ["5688UTC01R"], "rxcui": ["106303"], "spl_set_id": ["2b0c8ee4-83a5-48f1-809a-9716131f7290"], "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 (51672-1394-0)  / 20 g in 1 TUBE", "package_ndc": "51672-1394-0", "marketing_start_date": "20190125"}, {"sample": false, "description": "1 TUBE in 1 CARTON (51672-1394-9)  / 45 g in 1 TUBE", "package_ndc": "51672-1394-9", "marketing_start_date": "20190125"}], "brand_name": "Tretinoin", "product_id": "51672-1394_38ef297e-e4cb-0593-e063-6294a90a324d", "dosage_form": "CREAM", "pharm_class": ["Retinoid [EPC]", "Retinoids [CS]"], "product_ndc": "51672-1394", "generic_name": "tretinoin", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tretinoin", "active_ingredients": [{"name": "TRETINOIN", "strength": ".5 mg/g"}], "application_number": "ANDA211644", "marketing_category": "ANDA", "marketing_start_date": "20190125", "listing_expiration_date": "20261231"}