Package 72162-2215-0
Brand: glipizide
Generic: glipizidePackage Facts
Identity
Package NDC
72162-2215-0
Digits Only
7216222150
Product NDC
72162-2215
Description
1000 TABLET in 1 BOTTLE (72162-2215-0)
Marketing
Marketing Status
Brand
glipizide
Generic
glipizide
Sample Package
No
Linked Drug Pages (0)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0dbcf947-6edf-445a-b6b2-e1e76b9d78a8", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["X7WDT95N5C"], "rxcui": ["310488"], "spl_set_id": ["00729e82-150a-464a-abe7-a3319721fbdb"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (72162-2215-0)", "package_ndc": "72162-2215-0", "marketing_start_date": "20240105"}], "brand_name": "Glipizide", "product_id": "72162-2215_0dbcf947-6edf-445a-b6b2-e1e76b9d78a8", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "72162-2215", "generic_name": "Glipizide", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glipizide", "active_ingredients": [{"name": "GLIPIZIDE", "strength": "10 mg/1"}], "application_number": "ANDA074497", "marketing_category": "ANDA", "marketing_start_date": "20211213", "listing_expiration_date": "20261231"}