Package 70518-0104-0

Brand: glipizide

Generic: glipizide
NDC Package

Package Facts

Identity

Package NDC 70518-0104-0
Digits Only 7051801040
Product NDC 70518-0104
Description

30 TABLET in 1 BLISTER PACK (70518-0104-0)

Marketing

Marketing Status
Marketed Since 2017-01-09
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": "47e261d9-4e90-9c17-e063-6394a90a5412", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["X7WDT95N5C"], "rxcui": ["310490"], "spl_set_id": ["cfaef9c4-b243-4e27-ac92-3c319bc50ced"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-0104-0)", "package_ndc": "70518-0104-0", "marketing_start_date": "20170109"}], "brand_name": "Glipizide", "product_id": "70518-0104_47e261d9-4e90-9c17-e063-6394a90a5412", "dosage_form": "TABLET", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "70518-0104", "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": "ANDA075795", "marketing_category": "ANDA", "marketing_start_date": "20170109", "listing_expiration_date": "20271231"}