Package 70518-4128-1

Brand: glipizide

Generic: glipizide
NDC Package

Package Facts

Identity

Package NDC 70518-4128-1
Digits Only 7051841281
Product NDC 70518-4128
Description

90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4128-1)

Marketing

Marketing Status
Marketed Since 2025-09-08
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": "4cab0981-453a-ba61-e063-6294a90a699b", "openfda": {"nui": ["N0000175608", "M0020795"], "unii": ["X7WDT95N5C"], "spl_set_id": ["667dd68a-d3e7-4b50-bd0a-d17783a090d5"], "pharm_class_cs": ["Sulfonylurea Compounds [CS]"], "pharm_class_epc": ["Sulfonylurea [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4128-1)", "package_ndc": "70518-4128-1", "marketing_start_date": "20250908"}], "brand_name": "Glipizide", "product_id": "70518-4128_4cab0981-453a-ba61-e063-6294a90a699b", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Sulfonylurea Compounds [CS]", "Sulfonylurea [EPC]"], "product_ndc": "70518-4128", "generic_name": "Glipizide", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glipizide", "active_ingredients": [{"name": "GLIPIZIDE", "strength": "10 mg/1"}], "application_number": "ANDA206928", "marketing_category": "ANDA", "marketing_start_date": "20240701", "listing_expiration_date": "20271231"}