Package 72789-130-90

{"route": ["ORAL"], "spl_id": "4af77321-ff67-2bb7-e063-6394a90abecb", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["X7WDT95N5C"], "rxcui": ["310490"], "spl_set_id": ["f60b0690-aca9-40ec-956e-bd2ecc35ec54"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72789-130-30)", "package_ndc": "72789-130-30", "marketing_start_date": "20201123"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (72789-130-90)", "package_ndc": "72789-130-90", "marketing_start_date": "20201014"}], "brand_name": "Glipizide", "product_id": "72789-130_4af77321-ff67-2bb7-e063-6394a90abecb", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "72789-130", "generic_name": "Glipizide", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glipizide", "active_ingredients": [{"name": "GLIPIZIDE", "strength": "5 mg/1"}], "application_number": "ANDA075795", "marketing_category": "ANDA", "marketing_start_date": "20020925", "listing_expiration_date": "20271231"}