Package 68788-7856-1

{"route": ["ORAL"], "spl_id": "2d336d20-1f0a-450d-b7b8-3205f91ea802", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["X7WDT95N5C"], "rxcui": ["315107"], "spl_set_id": ["548c1f50-dbf0-49cc-b58b-fcc5937affa8"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7856-1)", "package_ndc": "68788-7856-1", "marketing_start_date": "20210129"}, {"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7856-3)", "package_ndc": "68788-7856-3", "marketing_start_date": "20210129"}, {"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7856-6)", "package_ndc": "68788-7856-6", "marketing_start_date": "20210129"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7856-9)", "package_ndc": "68788-7856-9", "marketing_start_date": "20210129"}], "brand_name": "Glipizide", "product_id": "68788-7856_2d336d20-1f0a-450d-b7b8-3205f91ea802", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "68788-7856", "generic_name": "Glipizide", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glipizide", "active_ingredients": [{"name": "GLIPIZIDE", "strength": "10 mg/1"}], "application_number": "ANDA204720", "marketing_category": "ANDA", "marketing_start_date": "20210129", "listing_expiration_date": "20261231"}