Package 50268-362-15
Brand: glipizide
Generic: glipizidePackage Facts
Identity
Package NDC
50268-362-15
Digits Only
5026836215
Product NDC
50268-362
Description
50 BLISTER PACK in 1 BOX (50268-362-15) / 1 TABLET in 1 BLISTER PACK (50268-362-11)
Marketing
Marketing Status
Brand
glipizide
Generic
glipizide
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "47e54668-1642-b614-e063-6294a90ad949", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["X7WDT95N5C"], "rxcui": ["310488", "310490"], "spl_set_id": ["aa1b16bf-e01c-d539-e053-2995a90a2735"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-362-15) / 1 TABLET in 1 BLISTER PACK (50268-362-11)", "package_ndc": "50268-362-15", "marketing_start_date": "20200710"}], "brand_name": "Glipizide", "product_id": "50268-362_47e54668-1642-b614-e063-6294a90ad949", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "50268-362", "generic_name": "Glipizide", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glipizide", "active_ingredients": [{"name": "GLIPIZIDE", "strength": "10 mg/1"}], "application_number": "ANDA075795", "marketing_category": "ANDA", "marketing_start_date": "20200710", "listing_expiration_date": "20271231"}