Package 70518-1063-1

{"route": ["ORAL"], "spl_id": "484b2c59-7af3-62c2-e063-6294a90ac3ac", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["X7WDT95N5C"], "rxcui": ["314006"], "spl_set_id": ["c2aadc88-22d2-467c-b2cb-03efb5a1f1c1"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-1063-0)", "package_ndc": "70518-1063-0", "marketing_start_date": "20180313"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-1063-1)", "package_ndc": "70518-1063-1", "marketing_start_date": "20180321"}], "brand_name": "Glipizide", "product_id": "70518-1063_484b2c59-7af3-62c2-e063-6294a90ac3ac", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "70518-1063", "generic_name": "Glipizide", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glipizide", "active_ingredients": [{"name": "GLIPIZIDE", "strength": "5 mg/1"}], "application_number": "ANDA204720", "marketing_category": "ANDA", "marketing_start_date": "20180313", "listing_expiration_date": "20271231"}